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Published in: Current Neurology and Neuroscience Reports 3/2017

01-03-2017 | Genetics (V Bonifati, Section Editor)

Update on the Genetics of Dystonia

Authors: Katja Lohmann, Christine Klein

Published in: Current Neurology and Neuroscience Reports | Issue 3/2017

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Abstract

Mainly due to the advent of next-generation sequencing (NGS), the field of genetics of dystonia has rapidly grown in recent years, which led to the discovery of a number of novel dystonia genes and the development of a new classification and nomenclature for inherited dystonias. In addition, new findings from both in vivo and in vitro studies have been published on the role of previously known dystonia genes, extending our understanding of the pathophysiology of dystonia. We here review the current knowledge and recent findings in the known genes for isolated dystonia TOR1A, THAP1, and GNAL as well as for the combined dystonias due to mutations in GCH1, ATP1A3, and SGCE. We present confirmatory evidence for a role of dystonia genes that had not yet been unequivocally established including PRKRA, TUBB4A, ANO3, and TAF1. We finally discuss selected novel genes for dystonia such as KMT2B and VAC14 along with the challenges for gene identification in the NGS era and the translational importance of dystonia genetics in clinical practice.
Literature
1.
go back to reference Oppenheim H. Ueber eigenenartige Krampfkrankheit des kindlichen und jugendlichen Alters (Dysbasia lordotica progressiva, Dystonia Musculorum Deformans). Neurol Centrabl. 1911;30:1090. Oppenheim H. Ueber eigenenartige Krampfkrankheit des kindlichen und jugendlichen Alters (Dysbasia lordotica progressiva, Dystonia Musculorum Deformans). Neurol Centrabl. 1911;30:1090.
2.
go back to reference • C. Klein, S. Fahn, Translation of Oppenheim’s 1911 paper on dystonia, Mov Disord 28 (2013) 851-862. This is a translation and commentary of Oppenheim’s landmark paper coining the term dystonia and most likely describing the first cases of generalized dystonia due to mutations in Tor1A (formerly DYT1) and suspecting a genetic etiology. • C. Klein, S. Fahn, Translation of Oppenheim’s 1911 paper on dystonia, Mov Disord 28 (2013) 851-862. This is a translation and commentary of Oppenheim’s landmark paper coining the term dystonia and most likely describing the first cases of generalized dystonia due to mutations in Tor1A (formerly DYT1) and suspecting a genetic etiology.
3.
go back to reference Steeves TD, Day L, Dykeman J, Jette N, Pringsheim T. The prevalence of primary dystonia: a systematic review and meta-analysis. Mov Disord. 2012;27:1789–96.CrossRefPubMed Steeves TD, Day L, Dykeman J, Jette N, Pringsheim T. The prevalence of primary dystonia: a systematic review and meta-analysis. Mov Disord. 2012;27:1789–96.CrossRefPubMed
4.
go back to reference • Albanese A, Bhatia K, Bressman SB, Delong MR, Fahn S, Fung VS, et al. Phenomenology and classification of dystonia: a consensus update. Mov Disord. 2013;28:863–73. This is an important paper that revises the definition and classification of dystonia based on a consensus outcome of an international expert panel. The new classification contains two axes: clinical characteristics and etiology. The latter one replaces the terms “primary” and “dystonia-plus” dystonia with “isolated” and “combined” dystonia, respectively.CrossRefPubMedPubMedCentral • Albanese A, Bhatia K, Bressman SB, Delong MR, Fahn S, Fung VS, et al. Phenomenology and classification of dystonia: a consensus update. Mov Disord. 2013;28:863–73. This is an important paper that revises the definition and classification of dystonia based on a consensus outcome of an international expert panel. The new classification contains two axes: clinical characteristics and etiology. The latter one replaces the terms “primary” and “dystonia-plus” dystonia with “isolated” and “combined” dystonia, respectively.CrossRefPubMedPubMedCentral
5.
go back to reference Wang L, Chen Y, Hu B, Hu X. Late-onset primary dystonia in Zhejiang province of China: a service-based epidemiological study. Neurol Sci. 2016;37:111–6.CrossRefPubMed Wang L, Chen Y, Hu B, Hu X. Late-onset primary dystonia in Zhejiang province of China: a service-based epidemiological study. Neurol Sci. 2016;37:111–6.CrossRefPubMed
6.
go back to reference L. Williams, E. McGovern, O. Kimmich, A. Molloy, I. Beiser, J.S. Butler, F. Molloy, P. Logan, D.G. Healy, T. Lynch, R. Walsh, L. Cassidy, P. Moriarty, H. Moore, T. McSwiney, C. Walsh, S. O’Riordan, M. Hutchinson, Epidemiological, clinical and genetic aspects of adult onset isolated focal dystonia in Ireland, Eur J Neurol (2016). L. Williams, E. McGovern, O. Kimmich, A. Molloy, I. Beiser, J.S. Butler, F. Molloy, P. Logan, D.G. Healy, T. Lynch, R. Walsh, L. Cassidy, P. Moriarty, H. Moore, T. McSwiney, C. Walsh, S. O’Riordan, M. Hutchinson, Epidemiological, clinical and genetic aspects of adult onset isolated focal dystonia in Ireland, Eur J Neurol (2016).
7.
go back to reference Molloy A, Williams L, Kimmich O, Butler JS, Beiser I, McGovern E, et al. Sun exposure is an environmental factor for the development of blepharospasm. J Neurol Neurosurg Psychiatry. 2016;87:420–4.CrossRefPubMed Molloy A, Williams L, Kimmich O, Butler JS, Beiser I, McGovern E, et al. Sun exposure is an environmental factor for the development of blepharospasm. J Neurol Neurosurg Psychiatry. 2016;87:420–4.CrossRefPubMed
8.
go back to reference Schmidt A, Jabusch HC, Altenmuller E, Hagenah J, Bruggemann N, Lohmann K, et al. Etiology of musician’s dystonia: familial or environmental? Neurology. 2009;72:1248–54.CrossRefPubMedPubMedCentral Schmidt A, Jabusch HC, Altenmuller E, Hagenah J, Bruggemann N, Lohmann K, et al. Etiology of musician’s dystonia: familial or environmental? Neurology. 2009;72:1248–54.CrossRefPubMedPubMedCentral
9.
go back to reference Groen JL, Kallen MC, van de Warrenburg BP, Speelman JD, van Hilten JJ, Aramideh M, et al. Phenotypes and genetic architecture of focal primary torsion dystonia. J Neurol Neurosurg Psychiatry. 2012;83:1006–11.CrossRefPubMed Groen JL, Kallen MC, van de Warrenburg BP, Speelman JD, van Hilten JJ, Aramideh M, et al. Phenotypes and genetic architecture of focal primary torsion dystonia. J Neurol Neurosurg Psychiatry. 2012;83:1006–11.CrossRefPubMed
10.
go back to reference van Egmond ME, Kuiper A, Eggink H, Sinke RJ, Brouwer OF, Verschuuren-Bemelmans CC, et al. Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm. J Neurol Neurosurg Psychiatry. 2015;86:774–81.CrossRefPubMed van Egmond ME, Kuiper A, Eggink H, Sinke RJ, Brouwer OF, Verschuuren-Bemelmans CC, et al. Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm. J Neurol Neurosurg Psychiatry. 2015;86:774–81.CrossRefPubMed
11.
go back to reference • M. Zech, S. Boesch, A. Jochim, S. Weber, T. Meindl, B. Schormair, T. Wieland, C. Lunetta, V. Sansone, M. Messner, J. Mueller, A. Ceballos-Baumann, T.M. Strom, R. Colombo, W. Poewe, B. Haslinger, J. Winkelmann, Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up, Mov Disord (2016). This is a relevant paper in two respects: first, it uses exome sequencing to detect the cause of dystonia in a small group of patients underlining the heterogeneity of dystonia. Second, it described the first de novo mutation in ANO3 providing increasing evidence for a pathogenic role of mutations in this gene. • M. Zech, S. Boesch, A. Jochim, S. Weber, T. Meindl, B. Schormair, T. Wieland, C. Lunetta, V. Sansone, M. Messner, J. Mueller, A. Ceballos-Baumann, T.M. Strom, R. Colombo, W. Poewe, B. Haslinger, J. Winkelmann, Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up, Mov Disord (2016). This is a relevant paper in two respects: first, it uses exome sequencing to detect the cause of dystonia in a small group of patients underlining the heterogeneity of dystonia. Second, it described the first de novo mutation in ANO3 providing increasing evidence for a pathogenic role of mutations in this gene.
12.
go back to reference •• Marras C, Lang A, van de Warrenburg BP, Sue CM, Tabrizi SJ, Bertram L, et al. Nomenclature of genetic movement disorders: recommendations of the international Parkinson and movement disorder society task force. Mov Disord. 2016;31:436–57. This paper is of major importance since it suggests a new nomenclature system for genetic movement disorders based on extensive considerations and discussions among an expert panel and members of the Movement Disorder Society.CrossRefPubMed •• Marras C, Lang A, van de Warrenburg BP, Sue CM, Tabrizi SJ, Bertram L, et al. Nomenclature of genetic movement disorders: recommendations of the international Parkinson and movement disorder society task force. Mov Disord. 2016;31:436–57. This paper is of major importance since it suggests a new nomenclature system for genetic movement disorders based on extensive considerations and discussions among an expert panel and members of the Movement Disorder Society.CrossRefPubMed
13.
go back to reference Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, et al. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nat Genet. 1997;17:40–8.CrossRefPubMed Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, et al. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nat Genet. 1997;17:40–8.CrossRefPubMed
14.
go back to reference Marras C, Lohmann K, Lang A, Klein C. Fixing the broken system of genetic locus symbols: Parkinson disease and dystonia as examples. Neurology. 2012;78:1016–24.CrossRefPubMedPubMedCentral Marras C, Lohmann K, Lang A, Klein C. Fixing the broken system of genetic locus symbols: Parkinson disease and dystonia as examples. Neurology. 2012;78:1016–24.CrossRefPubMedPubMedCentral
15.
go back to reference Domingo A, Erro R, Lohmann K. Novel dystonia genes: clues on disease mechanisms and the complexities of high-throughput sequencing. Mov Disord. 2016;31:471–7.CrossRefPubMed Domingo A, Erro R, Lohmann K. Novel dystonia genes: clues on disease mechanisms and the complexities of high-throughput sequencing. Mov Disord. 2016;31:471–7.CrossRefPubMed
16.
go back to reference Fuchs T, Gavarini S, Saunders-Pullman R, Raymond D, Ehrlich ME, Bressman SB, et al. Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nat Genet. 2009;41:286–8.CrossRefPubMed Fuchs T, Gavarini S, Saunders-Pullman R, Raymond D, Ehrlich ME, Bressman SB, et al. Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nat Genet. 2009;41:286–8.CrossRefPubMed
17.
go back to reference Fuchs T, Saunders-Pullman R, Masuho I, Luciano MS, Raymond D, Factor S, et al. Mutations in GNAL cause primary torsion dystonia. Nat Genet. 2013;45:88–92.CrossRefPubMed Fuchs T, Saunders-Pullman R, Masuho I, Luciano MS, Raymond D, Factor S, et al. Mutations in GNAL cause primary torsion dystonia. Nat Genet. 2013;45:88–92.CrossRefPubMed
18.
go back to reference Ichinose H, Ohye T, Takahashi E, Seki N, Hori T, Segawa M, et al. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nat Genet. 1994;8:236–42.CrossRefPubMed Ichinose H, Ohye T, Takahashi E, Seki N, Hori T, Segawa M, et al. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nat Genet. 1994;8:236–42.CrossRefPubMed
19.
go back to reference de Carvalho Aguiar P, Sweadner KJ, Penniston JT, Zaremba J, Liu L, Caton M, et al. Mutations in the Na+/K+-ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. Neuron. 2004;43:169–75.CrossRefPubMed de Carvalho Aguiar P, Sweadner KJ, Penniston JT, Zaremba J, Liu L, Caton M, et al. Mutations in the Na+/K+-ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. Neuron. 2004;43:169–75.CrossRefPubMed
20.
go back to reference Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, et al. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat Genet. 2001;29:66–9.CrossRefPubMed Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, et al. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat Genet. 2001;29:66–9.CrossRefPubMed
22.
go back to reference Bressman SB, Sabatti C, Raymond D, de Leon D, Klein C, Kramer PL, et al. The DYT1 phenotype and guidelines for diagnostic testing. Neurology. 2000;54:1746–52.CrossRefPubMed Bressman SB, Sabatti C, Raymond D, de Leon D, Klein C, Kramer PL, et al. The DYT1 phenotype and guidelines for diagnostic testing. Neurology. 2000;54:1746–52.CrossRefPubMed
23.
go back to reference Dobricic V, Kresojevic N, Zarkovic M, Tomic A, Marjanovic A, Westenberger A, et al. Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited. Parkinsonism Relat Disord. 2015;21:1256–9.CrossRefPubMed Dobricic V, Kresojevic N, Zarkovic M, Tomic A, Marjanovic A, Westenberger A, et al. Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited. Parkinsonism Relat Disord. 2015;21:1256–9.CrossRefPubMed
24.
go back to reference Vulinovic F, Lohmann K, Rakovic A, Capetian P, Alvarez-Fischer D, Schmidt A, et al. Unraveling cellular phenotypes of novel TorsinA/TOR1A mutations. Hum Mutat. 2014;35:1114–22.CrossRefPubMed Vulinovic F, Lohmann K, Rakovic A, Capetian P, Alvarez-Fischer D, Schmidt A, et al. Unraveling cellular phenotypes of novel TorsinA/TOR1A mutations. Hum Mutat. 2014;35:1114–22.CrossRefPubMed
25.
go back to reference Zech M, Jochim A, Boesch S, Weber S, Meindl T, Peters A, et al. Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls. Parkinsonism Relat Disord. 2016;31:119–23.CrossRefPubMed Zech M, Jochim A, Boesch S, Weber S, Meindl T, Peters A, et al. Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls. Parkinsonism Relat Disord. 2016;31:119–23.CrossRefPubMed
26.
go back to reference Hettich J, Ryan SD, de Souza ON, Saraiva Macedo Timmers LF, Tsai S, Atai NA, et al. Biochemical and cellular analysis of human variants of the DYT1 dystonia protein, TorsinA/TOR1A. Hum Mutat. 2014;35:1101–13.CrossRefPubMedPubMedCentral Hettich J, Ryan SD, de Souza ON, Saraiva Macedo Timmers LF, Tsai S, Atai NA, et al. Biochemical and cellular analysis of human variants of the DYT1 dystonia protein, TorsinA/TOR1A. Hum Mutat. 2014;35:1101–13.CrossRefPubMedPubMedCentral
27.
go back to reference Kabakci K, Hedrich K, Leung JC, Mitterer M, Vieregge P, Lencer R, et al. Mutations in DYT1: extension of the phenotypic and mutational spectrum. Neurology. 2004;62:395–400.CrossRefPubMed Kabakci K, Hedrich K, Leung JC, Mitterer M, Vieregge P, Lencer R, et al. Mutations in DYT1: extension of the phenotypic and mutational spectrum. Neurology. 2004;62:395–400.CrossRefPubMed
28.
go back to reference • Brüggemann N, Kühn A, Schneider SA, Kamm C, Wolters A, Krause P, et al. Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia. Neurology. 2015;84:895–903. This paper provides a translational aspect on the partially differential clinical outcome after deep brain stimulation in carriers of mutations in different dystonia genes. • Brüggemann N, Kühn A, Schneider SA, Kamm C, Wolters A, Krause P, et al. Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia. Neurology. 2015;84:895–903. This paper provides a translational aspect on the partially differential clinical outcome after deep brain stimulation in carriers of mutations in different dystonia genes.
29.
go back to reference Goodchild RE, Dauer WT. Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation. Proc Natl Acad Sci USA. 2004;101:847–52.CrossRefPubMedPubMedCentral Goodchild RE, Dauer WT. Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation. Proc Natl Acad Sci USA. 2004;101:847–52.CrossRefPubMedPubMedCentral
30.
go back to reference B.A. Sosa, F.E. Demircioglu, J.Z. Chen, J. Ingram, H.L. Ploegh, T.U. Schwartz, How lamina-associated polypeptide 1 (LAP1) activates Torsin, Elife 3 (2014) e03239. B.A. Sosa, F.E. Demircioglu, J.Z. Chen, J. Ingram, H.L. Ploegh, T.U. Schwartz, How lamina-associated polypeptide 1 (LAP1) activates Torsin, Elife 3 (2014) e03239.
31.
go back to reference Naismith TV, Dalal S, Hanson PI. Interaction of torsinA with its major binding partners is impaired by the dystonia-associated DeltaGAG deletion. J Biol Chem. 2009;284:27866–74.CrossRefPubMedPubMedCentral Naismith TV, Dalal S, Hanson PI. Interaction of torsinA with its major binding partners is impaired by the dystonia-associated DeltaGAG deletion. J Biol Chem. 2009;284:27866–74.CrossRefPubMedPubMedCentral
32.
go back to reference F.E. Demircioglu, B.A. Sosa, J. Ingram, H.L. Ploegh, T.U. Schwartz, Structures of TorsinA and its disease-mutant complexed with an activator reveal the molecular basis for primary dystonia, Elife 5 (2016). F.E. Demircioglu, B.A. Sosa, J. Ingram, H.L. Ploegh, T.U. Schwartz, Structures of TorsinA and its disease-mutant complexed with an activator reveal the molecular basis for primary dystonia, Elife 5 (2016).
33.
go back to reference •• Grillet M, Dominguez Gonzalez B, Sicart A, Pottler M, Cascalho A, Billion K, et al. Torsins are essential regulators of cellular lipid metabolism. Dev Cell. 2016;38:235–47. This is a very important study that links Torsin mutations to dysregulated cellular lipid metabolism and thus suggests a novel disease mechanism in dystonia. •• Grillet M, Dominguez Gonzalez B, Sicart A, Pottler M, Cascalho A, Billion K, et al. Torsins are essential regulators of cellular lipid metabolism. Dev Cell. 2016;38:235–47. This is a very important study that links Torsin mutations to dysregulated cellular lipid metabolism and thus suggests a novel disease mechanism in dystonia.
34.
go back to reference • V.G. Shakkottai, A. Batla, K. Bhatia, W.T. Dauer, C. Dresel, M. Niethammer, D. Eidelberg, R.S. Raike, Y. Smith, H.A. Jinnah, E.J. Hess, S. Meunier, M. Hallett, R. Fremont, K. Khodakhah, M.S. LeDoux, T. Popa, C. Gallea, S. Lehericy, A.C. Bostan, P.L. Strick, Current opinions and areas of consensus on the role of the cerebellum in dystonia, Cerebellum (2016). This is an important review summarizing and discussing data on the neuroanatomical site of origin of dystonia. It illustrates that the cerebellum plays a role in the pathophysiology of dystonia, but it is probably neither the primary nor sole relevant neuroanatomical structure. • V.G. Shakkottai, A. Batla, K. Bhatia, W.T. Dauer, C. Dresel, M. Niethammer, D. Eidelberg, R.S. Raike, Y. Smith, H.A. Jinnah, E.J. Hess, S. Meunier, M. Hallett, R. Fremont, K. Khodakhah, M.S. LeDoux, T. Popa, C. Gallea, S. Lehericy, A.C. Bostan, P.L. Strick, Current opinions and areas of consensus on the role of the cerebellum in dystonia, Cerebellum (2016). This is an important review summarizing and discussing data on the neuroanatomical site of origin of dystonia. It illustrates that the cerebellum plays a role in the pathophysiology of dystonia, but it is probably neither the primary nor sole relevant neuroanatomical structure.
35.
go back to reference E. Premi, M. Diano, S. Gazzina, F. Cauda, V. Gualeni, M. Tinazzi, M. Fiorio, P. Liberini, C. Lazzarini, S. Archetti, G. Biasotto, M. Turla, V. Bertasi, M. Cotelli, R. Gasparotti, A. Padovani, B. Borroni, Functional connectivity networks in asymptomatic and symptomatic DYT1 carriers, Mov Disord (2016). E. Premi, M. Diano, S. Gazzina, F. Cauda, V. Gualeni, M. Tinazzi, M. Fiorio, P. Liberini, C. Lazzarini, S. Archetti, G. Biasotto, M. Turla, V. Bertasi, M. Cotelli, R. Gasparotti, A. Padovani, B. Borroni, Functional connectivity networks in asymptomatic and symptomatic DYT1 carriers, Mov Disord (2016).
36.
go back to reference Vanni V, Puglisi F, Bonsi P, Ponterio G, Maltese M, Pisani A, et al. Cerebellar synaptogenesis is compromised in mouse models of DYT1 dystonia. Exp Neurol. 2015;271:457–67.CrossRefPubMed Vanni V, Puglisi F, Bonsi P, Ponterio G, Maltese M, Pisani A, et al. Cerebellar synaptogenesis is compromised in mouse models of DYT1 dystonia. Exp Neurol. 2015;271:457–67.CrossRefPubMed
37.
go back to reference Blanchard A, Ea V, Roubertie A, Martin M, Coquart C, Claustres M, et al. DYT6 dystonia: review of the literature and creation of the UMD Locus-Specific Database (LSDB) for mutations in the THAP1 gene. Hum Mutat. 2011;32:1213–24.CrossRefPubMed Blanchard A, Ea V, Roubertie A, Martin M, Coquart C, Claustres M, et al. DYT6 dystonia: review of the literature and creation of the UMD Locus-Specific Database (LSDB) for mutations in the THAP1 gene. Hum Mutat. 2011;32:1213–24.CrossRefPubMed
38.
go back to reference Lohmann K, Uflacker N, Erogullari A, Lohnau T, Winkler S, Dendorfer A, et al. Identification and functional analysis of novel THAP1 mutations. Eur J Hum Genet. 2012;20:171–5.CrossRefPubMed Lohmann K, Uflacker N, Erogullari A, Lohnau T, Winkler S, Dendorfer A, et al. Identification and functional analysis of novel THAP1 mutations. Eur J Hum Genet. 2012;20:171–5.CrossRefPubMed
39.
go back to reference Bressman SB, Raymond D, Fuchs T, Heiman GA, Ozelius LJ, Saunders-Pullman R. Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study. Lancet Neurol. 2009;8:441–6.CrossRefPubMedPubMedCentral Bressman SB, Raymond D, Fuchs T, Heiman GA, Ozelius LJ, Saunders-Pullman R. Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study. Lancet Neurol. 2009;8:441–6.CrossRefPubMedPubMedCentral
40.
go back to reference Paudel R, Li A, Hardy J, Bhatia KP, Houlden H, Holton J. DYT6 dystonia: a neuropathological study. Neurodegener Dis. 2016;16:273–8.CrossRefPubMed Paudel R, Li A, Hardy J, Bhatia KP, Houlden H, Holton J. DYT6 dystonia: a neuropathological study. Neurodegener Dis. 2016;16:273–8.CrossRefPubMed
41.
go back to reference Krause P, Bruggemann N, Volzmann S, Horn A, Kupsch A, Schneider GH, et al. Long-term effect on dystonia after pallidal deep brain stimulation (DBS) in three members of a family with a THAP1 mutation. J Neurol. 2015;262:2739–44.CrossRefPubMed Krause P, Bruggemann N, Volzmann S, Horn A, Kupsch A, Schneider GH, et al. Long-term effect on dystonia after pallidal deep brain stimulation (DBS) in three members of a family with a THAP1 mutation. J Neurol. 2015;262:2739–44.CrossRefPubMed
42.
go back to reference Ortiz-Virumbrales M, Ruiz M, Hone E, Dolios G, Wang R, Morant A, et al. Dystonia type 6 gene product Thap1: identification of a 50 kDa DNA-binding species in neuronal nuclear fractions. Acta Neuropathol Commun. 2014;2:139.CrossRefPubMedPubMedCentral Ortiz-Virumbrales M, Ruiz M, Hone E, Dolios G, Wang R, Morant A, et al. Dystonia type 6 gene product Thap1: identification of a 50 kDa DNA-binding species in neuronal nuclear fractions. Acta Neuropathol Commun. 2014;2:139.CrossRefPubMedPubMedCentral
43.
go back to reference Gavarini S, Cayrol C, Fuchs T, Lyons N, Ehrlich ME, Girard JP, et al. Direct interaction between causative genes of DYT1 and DYT6 primary dystonia. Ann Neurol. 2010;68:549–53.CrossRefPubMedPubMedCentral Gavarini S, Cayrol C, Fuchs T, Lyons N, Ehrlich ME, Girard JP, et al. Direct interaction between causative genes of DYT1 and DYT6 primary dystonia. Ann Neurol. 2010;68:549–53.CrossRefPubMedPubMedCentral
44.
go back to reference Kaiser FJ, Osmanoric A, Rakovic A, Erogullari A, Uflacker N, Braunholz D, et al. The dystonia gene DYT1 is repressed by the transcription factor THAP1. Ann Neurol. 2010;68:554–9. DYT6.CrossRefPubMed Kaiser FJ, Osmanoric A, Rakovic A, Erogullari A, Uflacker N, Braunholz D, et al. The dystonia gene DYT1 is repressed by the transcription factor THAP1. Ann Neurol. 2010;68:554–9. DYT6.CrossRefPubMed
45.
go back to reference LeDoux MS, Vemula SR, Xiao J, Thompson MM, Perlmutter JS, Wright LJ, et al. Clinical and genetic features of cervical dystonia in a large multicenter cohort. Neurol Genet. 2016;2:e69.CrossRefPubMedPubMedCentral LeDoux MS, Vemula SR, Xiao J, Thompson MM, Perlmutter JS, Wright LJ, et al. Clinical and genetic features of cervical dystonia in a large multicenter cohort. Neurol Genet. 2016;2:e69.CrossRefPubMedPubMedCentral
46.
go back to reference Vemula SR, Puschmann A, Xiao J, Zhao Y, Rudzinska M, Frei KP, et al. Role of Galpha(olf) in familial and sporadic adult-onset primary dystonia. Hum Mol Genet. 2013;22:2510–9.CrossRefPubMedPubMedCentral Vemula SR, Puschmann A, Xiao J, Zhao Y, Rudzinska M, Frei KP, et al. Role of Galpha(olf) in familial and sporadic adult-onset primary dystonia. Hum Mol Genet. 2013;22:2510–9.CrossRefPubMedPubMedCentral
47.
go back to reference • Masuho I, Fang M, Geng C, Zhang J, Jiang H, Ozgul RK, et al. Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia. Neurol Genet. 2016;2:e78. This is an interesting case report on a family with homozygous mutations in an actually dominantly inherited disorder. The data are not only descriptive on the phenotypic level but are accompanied by detailed functional analysis of the mutation underlining the importance of functional studies. • Masuho I, Fang M, Geng C, Zhang J, Jiang H, Ozgul RK, et al. Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia. Neurol Genet. 2016;2:e78. This is an interesting case report on a family with homozygous mutations in an actually dominantly inherited disorder. The data are not only descriptive on the phenotypic level but are accompanied by detailed functional analysis of the mutation underlining the importance of functional studies.
48.
go back to reference Opladen T, Hoffmann G, Horster F, Hinz AB, Neidhardt K, Klein C, et al. Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia. Mov Disord. 2011;26:157–61.CrossRefPubMed Opladen T, Hoffmann G, Horster F, Hinz AB, Neidhardt K, Klein C, et al. Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia. Mov Disord. 2011;26:157–61.CrossRefPubMed
49.
go back to reference Kumar KR, Lohmann K, Masuho I, Miyamoto R, Ferbert A, Lohnau T, et al. Mutations in GNAL: a novel cause of craniocervical dystonia. JAMA Neurol. 2014;71:490–4.CrossRefPubMedPubMedCentral Kumar KR, Lohmann K, Masuho I, Miyamoto R, Ferbert A, Lohnau T, et al. Mutations in GNAL: a novel cause of craniocervical dystonia. JAMA Neurol. 2014;71:490–4.CrossRefPubMedPubMedCentral
50.
go back to reference • Chen DH, Meneret A, Friedman JR, Korvatska O, Gad A, Bonkowski ES, et al. ADCY5-related dyskinesia: broader spectrum and genotype-phenotype correlations. Neurology. 2015;85:2026–35. This study reports many cases of ADCY5-related dyskinesia with a wide range of hyperkinetic abnormal movements. • Chen DH, Meneret A, Friedman JR, Korvatska O, Gad A, Bonkowski ES, et al. ADCY5-related dyskinesia: broader spectrum and genotype-phenotype correlations. Neurology. 2015;85:2026–35. This study reports many cases of ADCY5-related dyskinesia with a wide range of hyperkinetic abnormal movements.
51.
go back to reference V. Tadic, M. Kasten, N. Bruggemann, S. Stiller, J. Hagenah, C. Klein, Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signs, Arch Neurol (2012) 1-5. V. Tadic, M. Kasten, N. Bruggemann, S. Stiller, J. Hagenah, C. Klein, Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signs, Arch Neurol (2012) 1-5.
52.
go back to reference Lewthwaite AJ, Lambert TD, Rolfe EB, Olgiati S, Quadri M, Simons EJ, et al. Novel GCH1 variant in dopa-responsive dystonia and Parkinson’s disease. Parkinsonism Relat Disord. 2015;21:394–7.CrossRefPubMedPubMedCentral Lewthwaite AJ, Lambert TD, Rolfe EB, Olgiati S, Quadri M, Simons EJ, et al. Novel GCH1 variant in dopa-responsive dystonia and Parkinson’s disease. Parkinsonism Relat Disord. 2015;21:394–7.CrossRefPubMedPubMedCentral
53.
go back to reference Mencacci NE, Isaias IU, Reich MM, Ganos C, Plagnol V, Polke JM, et al. Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers. Brain. 2014;137:2480–92.CrossRefPubMedPubMedCentral Mencacci NE, Isaias IU, Reich MM, Ganos C, Plagnol V, Polke JM, et al. Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers. Brain. 2014;137:2480–92.CrossRefPubMedPubMedCentral
54.
go back to reference Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease. Nat Genet. 2014;46:989–93.CrossRefPubMedPubMedCentral Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease. Nat Genet. 2014;46:989–93.CrossRefPubMedPubMedCentral
55.
go back to reference Hagenah J, Saunders-Pullman R, Hedrich K, Kabakci K, Habermann K, Wiegers K, et al. High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening. Neurology. 2005;64:908–11.CrossRefPubMed Hagenah J, Saunders-Pullman R, Hedrich K, Kabakci K, Habermann K, Wiegers K, et al. High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening. Neurology. 2005;64:908–11.CrossRefPubMed
56.
go back to reference Douglas G, Hale AB, Crabtree MJ, Ryan BJ, Hansler A, Watschinger K, et al. A requirement for Gch1 and tetrahydrobiopterin in embryonic development. Dev Biol. 2015;399:129–38.CrossRefPubMedPubMedCentral Douglas G, Hale AB, Crabtree MJ, Ryan BJ, Hansler A, Watschinger K, et al. A requirement for Gch1 and tetrahydrobiopterin in embryonic development. Dev Biol. 2015;399:129–38.CrossRefPubMedPubMedCentral
57.
go back to reference Brüggemann N, Spiegler J, Hellenbroich Y, Opladen T, Schneider SA, Stephani U, et al. Beneficial prenatal levodopa therapy in autosomal recessive guanosine triphosphate cyclohydrolase 1 deficiency. Arch Neurol. 2012;69:1071–5.CrossRefPubMed Brüggemann N, Spiegler J, Hellenbroich Y, Opladen T, Schneider SA, Stephani U, et al. Beneficial prenatal levodopa therapy in autosomal recessive guanosine triphosphate cyclohydrolase 1 deficiency. Arch Neurol. 2012;69:1071–5.CrossRefPubMed
58.
go back to reference Brashear A, Dobyns WB, de Carvalho Aguiar P, Borg M, Frijns CJ, Gollamudi S, et al. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene. Brain. 2007;130:828–35.CrossRefPubMed Brashear A, Dobyns WB, de Carvalho Aguiar P, Borg M, Frijns CJ, Gollamudi S, et al. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene. Brain. 2007;130:828–35.CrossRefPubMed
59.
go back to reference • Sweney MT, Newcomb TM, Swoboda KJ. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, alternating hemiplegia of childhood, rapid-onset dystonia-parkinsonism, CAPOS and beyond. Pediatr Neurol. 2015;52:56–64. This important article illustrates the broad phenotypic spectrum of mutations in a single gene, i.e., ATP1A3. • Sweney MT, Newcomb TM, Swoboda KJ. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, alternating hemiplegia of childhood, rapid-onset dystonia-parkinsonism, CAPOS and beyond. Pediatr Neurol. 2015;52:56–64. This important article illustrates the broad phenotypic spectrum of mutations in a single gene, i.e., ATP1A3.
60.
go back to reference Holm TH, Isaksen TJ, Glerup S, Heuck A, Bottger P, Fuchtbauer EM, et al. Cognitive deficits caused by a disease-mutation in the alpha3 Na(+)/K(+)-ATPase isoform. Sci Rep. 2016;6:31972.CrossRefPubMedPubMedCentral Holm TH, Isaksen TJ, Glerup S, Heuck A, Bottger P, Fuchtbauer EM, et al. Cognitive deficits caused by a disease-mutation in the alpha3 Na(+)/K(+)-ATPase isoform. Sci Rep. 2016;6:31972.CrossRefPubMedPubMedCentral
61.
go back to reference M. Hully, J. Ropars, L. Hubert, N. Boddaert, M. Rio, M. Bernardelli, I. Desguerre, V. Cormier-Daire, A. Munnich, P. de Lonlay, L. Reilly, C. Besmond, N. Bahi-Buisson, Mosaicism in ATP1A3-related disorders: not just a theoretical risk, Neurogenetics (2016). M. Hully, J. Ropars, L. Hubert, N. Boddaert, M. Rio, M. Bernardelli, I. Desguerre, V. Cormier-Daire, A. Munnich, P. de Lonlay, L. Reilly, C. Besmond, N. Bahi-Buisson, Mosaicism in ATP1A3-related disorders: not just a theoretical risk, Neurogenetics (2016).
62.
go back to reference Grünewald A, Djarmati A, Lohmann-Hedrich K, Farrell K, Zeller JA, Allert N, et al. Myoclonus-dystonia: significance of large SGCE deletions. Hum Mutat. 2008;29:331–2.CrossRefPubMed Grünewald A, Djarmati A, Lohmann-Hedrich K, Farrell K, Zeller JA, Allert N, et al. Myoclonus-dystonia: significance of large SGCE deletions. Hum Mutat. 2008;29:331–2.CrossRefPubMed
63.
go back to reference Peall KJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, et al. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. J Neurol. 2014;261:2296–304.CrossRefPubMedPubMedCentral Peall KJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, et al. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. J Neurol. 2014;261:2296–304.CrossRefPubMedPubMedCentral
64.
go back to reference Peall KJ, Dijk JM, Saunders-Pullman R, Dreissen YE, van Loon I, Cath D, et al. Psychiatric disorders, myoclonus dystonia and SGCE: an international study. Ann Clin Transl Neurol. 2016;3:4–11.CrossRefPubMed Peall KJ, Dijk JM, Saunders-Pullman R, Dreissen YE, van Loon I, Cath D, et al. Psychiatric disorders, myoclonus dystonia and SGCE: an international study. Ann Clin Transl Neurol. 2016;3:4–11.CrossRefPubMed
65.
go back to reference Müller B, Hedrich K, Kock N, Dragasevic N, Svetel M, Garrels J, et al. Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia. Am J Hum Genet. 2002;71:1303–11.CrossRefPubMedPubMedCentral Müller B, Hedrich K, Kock N, Dragasevic N, Svetel M, Garrels J, et al. Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia. Am J Hum Genet. 2002;71:1303–11.CrossRefPubMedPubMedCentral
66.
go back to reference Hack AA, Groh ME, McNally EM. Sarcoglycans in muscular dystrophy. Microsc Res Tech. 2000;48:167–80.CrossRefPubMed Hack AA, Groh ME, McNally EM. Sarcoglycans in muscular dystrophy. Microsc Res Tech. 2000;48:167–80.CrossRefPubMed
67.
go back to reference • Boulay AC, Saubamea B, Cisternino S, Mignon V, Mazeraud A, Jourdren L, et al. The sarcoglycan complex is expressed in the cerebrovascular system and is specifically regulated by astroglial Cx30 channels. Front Cell Neurosci. 2015;9:9. This functional study highlights a potential disease mechanism of mutations in the SGCE gene by linking the sarcoglycan complex to the cerebrovascular system. • Boulay AC, Saubamea B, Cisternino S, Mignon V, Mazeraud A, Jourdren L, et al. The sarcoglycan complex is expressed in the cerebrovascular system and is specifically regulated by astroglial Cx30 channels. Front Cell Neurosci. 2015;9:9. This functional study highlights a potential disease mechanism of mutations in the SGCE gene by linking the sarcoglycan complex to the cerebrovascular system.
68.
go back to reference •• A. Keller, A. Westenberger, M.J. Sobrido, M. Garcia-Murias, A. Domingo, R.L. Sears, R.R. Lemos, A. Ordonez-Ugalde, G. Nicolas, J.E. da Cunha, E.J. Rushing, M. Hugelshofer, M.C. Wurnig, A. Kaech, R. Reimann, K. Lohmann, V. Dobricic, A. Carracedo, I. Petrovic, J.M. Miyasaki, I. Abakumova, M.A. Mae, E. Raschperger, M. Zatz, K. Zschiedrich, J. Klepper, E. Spiteri, J.M. Prieto, I. Navas, M. Preuss, C. Dering, M. Jankovic, M. Paucar, P. Svenningsson, K. Saliminejad, H.R. Khorshid, I. Novakovic, A. Aguzzi, A. Boss, I. Le Ber, G. Defer, D. Hannequin, V.S. Kostic, D. Campion, D.H. Geschwind, G. Coppola, C. Betsholtz, C. Klein, J.R. Oliveira, Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice, Nat Genet (2013). This comprehensive study elucidated a frequent cause of primary familial brain calcification by identification of mutations in the PDGFB gene. It not only reported the cause of the disease in several multiplex families but also demonstrated corresponding brain calcifications in mouse models at different ages and linked this complex form of dystonia to dysfunction of the blood brain barrier. •• A. Keller, A. Westenberger, M.J. Sobrido, M. Garcia-Murias, A. Domingo, R.L. Sears, R.R. Lemos, A. Ordonez-Ugalde, G. Nicolas, J.E. da Cunha, E.J. Rushing, M. Hugelshofer, M.C. Wurnig, A. Kaech, R. Reimann, K. Lohmann, V. Dobricic, A. Carracedo, I. Petrovic, J.M. Miyasaki, I. Abakumova, M.A. Mae, E. Raschperger, M. Zatz, K. Zschiedrich, J. Klepper, E. Spiteri, J.M. Prieto, I. Navas, M. Preuss, C. Dering, M. Jankovic, M. Paucar, P. Svenningsson, K. Saliminejad, H.R. Khorshid, I. Novakovic, A. Aguzzi, A. Boss, I. Le Ber, G. Defer, D. Hannequin, V.S. Kostic, D. Campion, D.H. Geschwind, G. Coppola, C. Betsholtz, C. Klein, J.R. Oliveira, Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice, Nat Genet (2013). This comprehensive study elucidated a frequent cause of primary familial brain calcification by identification of mutations in the PDGFB gene. It not only reported the cause of the disease in several multiplex families but also demonstrated corresponding brain calcifications in mouse models at different ages and linked this complex form of dystonia to dysfunction of the blood brain barrier.
69.
go back to reference Nicolas G, Pottier C, Maltete D, Coutant S, Rovelet-Lecrux A, Legallic S, et al. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification. Neurology. 2013;80:181–7.CrossRefPubMed Nicolas G, Pottier C, Maltete D, Coutant S, Rovelet-Lecrux A, Legallic S, et al. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification. Neurology. 2013;80:181–7.CrossRefPubMed
70.
go back to reference Westenberger A, Klein C. The genetics of primary familial brain calcifications. Curr Neurol Neurosci Rep. 2014;14:490.CrossRefPubMed Westenberger A, Klein C. The genetics of primary familial brain calcifications. Curr Neurol Neurosci Rep. 2014;14:490.CrossRefPubMed
71.
go back to reference Camargos S, Scholz S, Simon-Sanchez J, Paisan-Ruiz C, Lewis P, Hernandez D, et al. DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA. Lancet Neurol. 2008;7:207–15.CrossRefPubMed Camargos S, Scholz S, Simon-Sanchez J, Paisan-Ruiz C, Lewis P, Hernandez D, et al. DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA. Lancet Neurol. 2008;7:207–15.CrossRefPubMed
72.
go back to reference Hersheson J, Mencacci NE, Davis M, Macdonald N, Trabzuni D, Ryten M, et al. Mutations in the autoregulatory domain of beta-tubulin 4a cause hereditary dystonia. Ann Neurol. 2013;73:546–53.CrossRefPubMedPubMedCentral Hersheson J, Mencacci NE, Davis M, Macdonald N, Trabzuni D, Ryten M, et al. Mutations in the autoregulatory domain of beta-tubulin 4a cause hereditary dystonia. Ann Neurol. 2013;73:546–53.CrossRefPubMedPubMedCentral
73.
go back to reference Lohmann K, Wilcox RA, Winkler S, Ramirez A, Rakovic A, Park JS, et al. Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene. Ann Neurol. 2013;73:537–45.CrossRefPubMed Lohmann K, Wilcox RA, Winkler S, Ramirez A, Rakovic A, Park JS, et al. Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene. Ann Neurol. 2013;73:537–45.CrossRefPubMed
74.
go back to reference Charlesworth G, Plagnol V, Holmstrom KM, Bras J, Sheerin UM, Preza E, et al. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis. Am J Hum Genet. 2012;91:1041–50.CrossRefPubMedPubMedCentral Charlesworth G, Plagnol V, Holmstrom KM, Bras J, Sheerin UM, Preza E, et al. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis. Am J Hum Genet. 2012;91:1041–50.CrossRefPubMedPubMedCentral
75.
go back to reference Zech M, Gross N, Jochim A, Castrop F, Kaffe M, Dresel C, et al. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls. Mov Disord. 2014;29:143–7.CrossRefPubMed Zech M, Gross N, Jochim A, Castrop F, Kaffe M, Dresel C, et al. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls. Mov Disord. 2014;29:143–7.CrossRefPubMed
76.
go back to reference Nolte D, Niemann S, Muller U. Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism. Proc Natl Acad Sci USA. 2003;100:10347–52.CrossRefPubMedPubMedCentral Nolte D, Niemann S, Muller U. Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism. Proc Natl Acad Sci USA. 2003;100:10347–52.CrossRefPubMedPubMedCentral
77.
go back to reference • Quadri M, Olgiati S, Sensi M, Gualandi F, Groppo E, Rispoli V, et al. PRKRA mutation causing early-onset generalized dystonia-parkinsonism (DYT16) in an Italian family. Mov Disord. 2016;31:765–7. This interesting paper confirms biallelic mutations in the PRKRA gene as a cause of dystonia-parkinsonism and demonstrates a founder effect. • Quadri M, Olgiati S, Sensi M, Gualandi F, Groppo E, Rispoli V, et al. PRKRA mutation causing early-onset generalized dystonia-parkinsonism (DYT16) in an Italian family. Mov Disord. 2016;31:765–7. This interesting paper confirms biallelic mutations in the PRKRA gene as a cause of dystonia-parkinsonism and demonstrates a founder effect.
78.
go back to reference Wilcox RA, Winkler S, Lohmann K, Klein C. Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal. Mov Disord. 2011;26:2404–8.CrossRefPubMed Wilcox RA, Winkler S, Lohmann K, Klein C. Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal. Mov Disord. 2011;26:2404–8.CrossRefPubMed
79.
go back to reference Zech M, Boesch S, Jochim A, Graf S, Lichtner P, Peters A, et al. Large-scale TUBB4A mutational screening in isolated dystonia and controls. Parkinsonism Relat Disord. 2015;21:1278–81.CrossRefPubMed Zech M, Boesch S, Jochim A, Graf S, Lichtner P, Peters A, et al. Large-scale TUBB4A mutational screening in isolated dystonia and controls. Parkinsonism Relat Disord. 2015;21:1278–81.CrossRefPubMed
80.
go back to reference Erro R, Hersheson J, Ganos C, Mencacci NE, Stamelou M, Batla A, et al. H-ABC syndrome and DYT4: variable expressivity or pleiotropy of TUBB4 mutations? Mov Disord. 2015;30:828–33.CrossRefPubMed Erro R, Hersheson J, Ganos C, Mencacci NE, Stamelou M, Batla A, et al. H-ABC syndrome and DYT4: variable expressivity or pleiotropy of TUBB4 mutations? Mov Disord. 2015;30:828–33.CrossRefPubMed
81.
go back to reference Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17:405–24.CrossRefPubMedPubMedCentral Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17:405–24.CrossRefPubMedPubMedCentral
82.
go back to reference Lee LV, Pascasio FM, Fuentes FD, Viterbo GH. Torsion dystonia in Panay. Philippines Adv Neurol. 1976;14:137–51.PubMed Lee LV, Pascasio FM, Fuentes FD, Viterbo GH. Torsion dystonia in Panay. Philippines Adv Neurol. 1976;14:137–51.PubMed
83.
go back to reference Domingo A, Westenberger A, Lee LV, Braenne I, Liu T, Vater I, et al. New insights into the genetics of X-linked dystonia-parkinsonism. Eur J Hum Genet. 2015;23:1334–40. XDP, DYT3.CrossRefPubMedPubMedCentral Domingo A, Westenberger A, Lee LV, Braenne I, Liu T, Vater I, et al. New insights into the genetics of X-linked dystonia-parkinsonism. Eur J Hum Genet. 2015;23:1334–40. XDP, DYT3.CrossRefPubMedPubMedCentral
84.
go back to reference Domingo A, Amar D, Grutz K, Lee LV, Rosales R, Bruggemann N, et al. Evidence of TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonism. Cell Mol Life Sci. 2016;73:3205–15.CrossRefPubMed Domingo A, Amar D, Grutz K, Lee LV, Rosales R, Bruggemann N, et al. Evidence of TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonism. Cell Mol Life Sci. 2016;73:3205–15.CrossRefPubMed
85.
go back to reference •• J.A. O’Rawe, Y. Wu, M.J. Dorfel, A.F. Rope, P.Y. Au, J.S. Parboosingh, S. Moon, M. Kousi, K. Kosma, C.S. Smith, M. Tzetis, J.L. Schuette, R.B. Hufnagel, C.E. Prada, F. Martinez, C. Orellana, J. Crain, A. Caro-Llopis, S. Oltra, S. Monfort, L.T. Jimenez-Barron, J. Swensen, S. Ellingwood, R. Smith, H. Fang, S. Ospina, S. Stegmann, N. Den Hollander, D. Mittelman, G. Highnam, R. Robison, E. Yang, L. Faivre, A. Roubertie, J.B. Riviere, K.G. Monaghan, K. Wang, E.E. Davis, N. Katsanis, V.M. Kalscheuer, E.H. Wang, K. Metcalfe, T. Kleefstra, A.M. Innes, S. Kitsiou-Tzeli, M. Rosello, C.E. Keegan, G.J. Lyon, TAF1 variants are associated with dysmorphic features, intellectual disability, and neurological manifestations, Am J Hum Genet 97 (2015) 922-932. This manuscript describes bona fide mutations in the TAF1 gene, the gene that is also dysregulated in X-linked dystonia-parkinsonism (XDP) due to several disease-specific changes. •• J.A. O’Rawe, Y. Wu, M.J. Dorfel, A.F. Rope, P.Y. Au, J.S. Parboosingh, S. Moon, M. Kousi, K. Kosma, C.S. Smith, M. Tzetis, J.L. Schuette, R.B. Hufnagel, C.E. Prada, F. Martinez, C. Orellana, J. Crain, A. Caro-Llopis, S. Oltra, S. Monfort, L.T. Jimenez-Barron, J. Swensen, S. Ellingwood, R. Smith, H. Fang, S. Ospina, S. Stegmann, N. Den Hollander, D. Mittelman, G. Highnam, R. Robison, E. Yang, L. Faivre, A. Roubertie, J.B. Riviere, K.G. Monaghan, K. Wang, E.E. Davis, N. Katsanis, V.M. Kalscheuer, E.H. Wang, K. Metcalfe, T. Kleefstra, A.M. Innes, S. Kitsiou-Tzeli, M. Rosello, C.E. Keegan, G.J. Lyon, TAF1 variants are associated with dysmorphic features, intellectual disability, and neurological manifestations, Am J Hum Genet 97 (2015) 922-932. This manuscript describes bona fide mutations in the TAF1 gene, the gene that is also dysregulated in X-linked dystonia-parkinsonism (XDP) due to several disease-specific changes.
86.
go back to reference Hagenah JM, Zuhlke C, Hellenbroich Y, Heide W, Klein C. Focal dystonia as a presenting sign of spinocerebellar ataxia 17. Mov Disord. 2004;19:217–20.CrossRefPubMed Hagenah JM, Zuhlke C, Hellenbroich Y, Heide W, Klein C. Focal dystonia as a presenting sign of spinocerebellar ataxia 17. Mov Disord. 2004;19:217–20.CrossRefPubMed
87.
go back to reference Chen YZ, Matsushita MM, Robertson P, Rieder M, Girirajan S, Antonacci F, et al. Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5. Arch Neurol. 2012;69:630–5.CrossRefPubMedPubMedCentral Chen YZ, Matsushita MM, Robertson P, Rieder M, Girirajan S, Antonacci F, et al. Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5. Arch Neurol. 2012;69:630–5.CrossRefPubMedPubMedCentral
88.
go back to reference Carapito R, Paul N, Untrau M, Le Gentil M, Ott L, Alsaleh G, et al. A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia. Mov Disord. 2015;30:423–7.CrossRefPubMed Carapito R, Paul N, Untrau M, Le Gentil M, Ott L, Alsaleh G, et al. A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia. Mov Disord. 2015;30:423–7.CrossRefPubMed
89.
go back to reference F.C. Chang, A. Westenberger, R.C. Dale, M. Smith, H.S. Pall, B. Perez-Duenas, P. Grattan-Smith, R.A. Ouvrier, N. Mahant, B.C. Hanna, M. Hunter, J.A. Lawson, C. Max, R. Sachdev, E. Meyer, D. Crimmins, D. Pryor, J.G. Morris, A. Munchau, D. Grozeva, K.J. Carss, L. Raymond, M.A. Kurian, C. Klein, V.S. Fung, Phenotypic insights into ADCY5-associated disease, Mov Disord (2016). F.C. Chang, A. Westenberger, R.C. Dale, M. Smith, H.S. Pall, B. Perez-Duenas, P. Grattan-Smith, R.A. Ouvrier, N. Mahant, B.C. Hanna, M. Hunter, J.A. Lawson, C. Max, R. Sachdev, E. Meyer, D. Crimmins, D. Pryor, J.G. Morris, A. Munchau, D. Grozeva, K.J. Carss, L. Raymond, M.A. Kurian, C. Klein, V.S. Fung, Phenotypic insights into ADCY5-associated disease, Mov Disord (2016).
90.
go back to reference •• S. Petrovski, S. Kury, C.T. Myers, K. Anyane-Yeboa, B. Cogne, M. Bialer, F. Xia, P. Hemati, J. Riviello, M. Mehaffey, T. Besnard, E. Becraft, A. Wadley, A.R. Politi, S. Colombo, X. Zhu, Z. Ren, I. Andrews, T. Dudding-Byth, A.L. Schneider, G. Wallace, A.B. Rosen, S. Schelley, G.M. Enns, P. Corre, J. Dalton, S. Mercier, X. Latypova, S. Schmitt, E. Guzman, C. Moore, L. Bier, E.L. Heinzen, P. Karachunski, N. Shur, T. Grebe, A. Basinger, J.M. Nguyen, S. Bezieau, K. Wierenga, J.A. Bernstein, I.E. Scheffer, J.A. Rosenfeld, H.C. Mefford, B. Isidor, D.B. Goldstein, Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures, Am J Hum Genet 98 (2016) 1001-1010. This nicely performed screening study elucidated mutations in the GNB1 gene as a rare but recurrent cause of a complex form of dystonia and highlights G protein-mediated signaling as one disease mechanism in dystonia and neurodevelopmental disability. •• S. Petrovski, S. Kury, C.T. Myers, K. Anyane-Yeboa, B. Cogne, M. Bialer, F. Xia, P. Hemati, J. Riviello, M. Mehaffey, T. Besnard, E. Becraft, A. Wadley, A.R. Politi, S. Colombo, X. Zhu, Z. Ren, I. Andrews, T. Dudding-Byth, A.L. Schneider, G. Wallace, A.B. Rosen, S. Schelley, G.M. Enns, P. Corre, J. Dalton, S. Mercier, X. Latypova, S. Schmitt, E. Guzman, C. Moore, L. Bier, E.L. Heinzen, P. Karachunski, N. Shur, T. Grebe, A. Basinger, J.M. Nguyen, S. Bezieau, K. Wierenga, J.A. Bernstein, I.E. Scheffer, J.A. Rosenfeld, H.C. Mefford, B. Isidor, D.B. Goldstein, Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures, Am J Hum Genet 98 (2016) 1001-1010. This nicely performed screening study elucidated mutations in the GNB1 gene as a rare but recurrent cause of a complex form of dystonia and highlights G protein-mediated signaling as one disease mechanism in dystonia and neurodevelopmental disability.
91.
go back to reference Steinrucke S, Lohmann K, Domingo A, Rolfs A, Baumer T, Spiegler J, et al. Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability. Neurol Genet. 2016;2:e106.CrossRefPubMedPubMedCentral Steinrucke S, Lohmann K, Domingo A, Rolfs A, Baumer T, Spiegler J, et al. Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability. Neurol Genet. 2016;2:e106.CrossRefPubMedPubMedCentral
92.
go back to reference L.A. Menke, M. Engelen, M. Alders, V.J. Odekerken, F. Baas, J.M. Cobben, Recurrent GNAO1 mutations associated with developmental delay and a movement disorder, J Child Neurol (2016). L.A. Menke, M. Engelen, M. Alders, V.J. Odekerken, F. Baas, J.M. Cobben, Recurrent GNAO1 mutations associated with developmental delay and a movement disorder, J Child Neurol (2016).
93.
go back to reference Nakamura K, Kodera H, Akita T, Shiina M, Kato M, Hoshino H, et al. De Novo mutations in GNAO1, encoding a Galphao subunit of heterotrimeric G proteins, cause epileptic encephalopathy. Am J Hum Genet. 2013;93:496–505.CrossRefPubMedPubMedCentral Nakamura K, Kodera H, Akita T, Shiina M, Kato M, Hoshino H, et al. De Novo mutations in GNAO1, encoding a Galphao subunit of heterotrimeric G proteins, cause epileptic encephalopathy. Am J Hum Genet. 2013;93:496–505.CrossRefPubMedPubMedCentral
94.
go back to reference Lenk GM, Szymanska K, Debska-Vielhaber G, Rydzanicz M, Walczak A, Bekiesinska-Figatowska M, et al. Biallelic mutations of VAC14 in pediatric-onset neurological disease. Am J Hum Genet. 2016;99:188–94.CrossRefPubMedPubMedCentral Lenk GM, Szymanska K, Debska-Vielhaber G, Rydzanicz M, Walczak A, Bekiesinska-Figatowska M, et al. Biallelic mutations of VAC14 in pediatric-onset neurological disease. Am J Hum Genet. 2016;99:188–94.CrossRefPubMedPubMedCentral
95.
go back to reference S. Edvardson, G. Tian, H. Cullen, H. Vanyai, L. Ngo, S. Bhat, A. Aran, M. Daana, N. Da’amseh, B. Abu-Libdeh, N.J. Cowan, J. Heng, O. Elpeleg, Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway, Hum Mol Genet (2016). S. Edvardson, G. Tian, H. Cullen, H. Vanyai, L. Ngo, S. Bhat, A. Aran, M. Daana, N. Da’amseh, B. Abu-Libdeh, N.J. Cowan, J. Heng, O. Elpeleg, Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway, Hum Mol Genet (2016).
96.
go back to reference •• Zech M, Boesch S, Maier EM, Borggraefe I, Vill K, Laccone F, et al. Haploinsufficiency of KMT2B, encoding the lysine-specific histone methyltransferase 2B, results in early-onset generalized dystonia. Am J Hum Genet. 2016;99:1377–87. This paper represents one of the two studies elucidating KMT2B mutations as a relatively common cause of early-onset dystonia.CrossRefPubMed •• Zech M, Boesch S, Maier EM, Borggraefe I, Vill K, Laccone F, et al. Haploinsufficiency of KMT2B, encoding the lysine-specific histone methyltransferase 2B, results in early-onset generalized dystonia. Am J Hum Genet. 2016;99:1377–87. This paper represents one of the two studies elucidating KMT2B mutations as a relatively common cause of early-onset dystonia.CrossRefPubMed
97.
go back to reference •• E. Meyer, K.J. Carss, J. Rankin, J.M. Nichols, D. Grozeva, A.P. Joseph, N.E. Mencacci, A. Papandreou, J. Ng, S. Barral, A. Ngoh, H. Ben-Pazi, M.A. Willemsen, D. Arkadir, A. Barnicoat, H. Bergman, S. Bhate, A. Boys, N. Darin, N. Foulds, N. Gutowski, A. Hills, H. Houlden, J.A. Hurst, Z. Israel, M. Kaminska, P. Limousin, D. Lumsden, S. McKee, S. Misra, S.S. Mohammed, V. Nakou, J. Nicolai, M. Nilsson, H. Pall, K.J. Peall, G.B. Peters, P. Prabhakar, M.S. Reuter, P. Rump, R. Segel, M. Sinnema, M. Smith, P. Turnpenny, S.M. White, D. Wieczorek, S. Wiethoff, B.T. Wilson, G. Winter, C. Wragg, S. Pope, S.J. Heales, D. Morrogh, A. Pittman, L.J. Carr, B. Perez-Duenas, J.P. Lin, A. Reis, W.A. Gahl, C. Toro, K.P. Bhatia, N.W. Wood, E.J. Kamsteeg, W.K. Chong, P. Gissen, M. Topf, R.C. Dale, J.R. Chubb, F.L. Raymond, M.A. Kurian, Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia, Nat Genet (2016). This paper represents one of the two studies elucidating KMT2B mutations as a relatively common cause of early-onset dystonia. •• E. Meyer, K.J. Carss, J. Rankin, J.M. Nichols, D. Grozeva, A.P. Joseph, N.E. Mencacci, A. Papandreou, J. Ng, S. Barral, A. Ngoh, H. Ben-Pazi, M.A. Willemsen, D. Arkadir, A. Barnicoat, H. Bergman, S. Bhate, A. Boys, N. Darin, N. Foulds, N. Gutowski, A. Hills, H. Houlden, J.A. Hurst, Z. Israel, M. Kaminska, P. Limousin, D. Lumsden, S. McKee, S. Misra, S.S. Mohammed, V. Nakou, J. Nicolai, M. Nilsson, H. Pall, K.J. Peall, G.B. Peters, P. Prabhakar, M.S. Reuter, P. Rump, R. Segel, M. Sinnema, M. Smith, P. Turnpenny, S.M. White, D. Wieczorek, S. Wiethoff, B.T. Wilson, G. Winter, C. Wragg, S. Pope, S.J. Heales, D. Morrogh, A. Pittman, L.J. Carr, B. Perez-Duenas, J.P. Lin, A. Reis, W.A. Gahl, C. Toro, K.P. Bhatia, N.W. Wood, E.J. Kamsteeg, W.K. Chong, P. Gissen, M. Topf, R.C. Dale, J.R. Chubb, F.L. Raymond, M.A. Kurian, Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia, Nat Genet (2016). This paper represents one of the two studies elucidating KMT2B mutations as a relatively common cause of early-onset dystonia.
98.
go back to reference K. Lohmann, C. Klein, Next generation sequencing and the future of genetic diagnosis, Neurotherapeutics (2014). K. Lohmann, C. Klein, Next generation sequencing and the future of genetic diagnosis, Neurotherapeutics (2014).
99.
go back to reference Olgiati S, Quadri M, Bonifati V. Genetics of movement disorders in the next-generation sequencing era. Mov Disord. 2016;31:458–70.CrossRefPubMed Olgiati S, Quadri M, Bonifati V. Genetics of movement disorders in the next-generation sequencing era. Mov Disord. 2016;31:458–70.CrossRefPubMed
100.
go back to reference Mencacci NE, R’Bibo L, Bandres-Ciga S, Carecchio M, Zorzi G, Nardocci N, et al. The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort. Hum Mol Genet. 2015;24:5326–9.CrossRefPubMedPubMedCentral Mencacci NE, R’Bibo L, Bandres-Ciga S, Carecchio M, Zorzi G, Nardocci N, et al. The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort. Hum Mol Genet. 2015;24:5326–9.CrossRefPubMedPubMedCentral
101.
go back to reference Lohmann K, Klein C. Genetics of dystonia: what’s known? what’s new? what’s next? Mov Disord. 2013;28:899–905.CrossRefPubMed Lohmann K, Klein C. Genetics of dystonia: what’s known? what’s new? what’s next? Mov Disord. 2013;28:899–905.CrossRefPubMed
102.
go back to reference Mok KY, Schneider SA, Trabzuni D, Stamelou M, Edwards M, Kasperaviciute D, et al. Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel. Mov Disord. 2014;29:245–51.CrossRefPubMed Mok KY, Schneider SA, Trabzuni D, Stamelou M, Edwards M, Kasperaviciute D, et al. Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel. Mov Disord. 2014;29:245–51.CrossRefPubMed
103.
go back to reference Lohmann K, Schmidt A, Schillert A, Winkler S, Albanese A, Baas F, et al. Genome-wide association study in musician’s dystonia: a risk variant at the arylsulfatase G locus? Mov Disord. 2014;29:921–7.CrossRefPubMed Lohmann K, Schmidt A, Schillert A, Winkler S, Albanese A, Baas F, et al. Genome-wide association study in musician’s dystonia: a risk variant at the arylsulfatase G locus? Mov Disord. 2014;29:921–7.CrossRefPubMed
104.
go back to reference Veltman JA, Brunner HG. De novo mutations in human genetic disease. Nat Rev Genet. 2012;13:565–75.CrossRefPubMed Veltman JA, Brunner HG. De novo mutations in human genetic disease. Nat Rev Genet. 2012;13:565–75.CrossRefPubMed
Metadata
Title
Update on the Genetics of Dystonia
Authors
Katja Lohmann
Christine Klein
Publication date
01-03-2017
Publisher
Springer US
Published in
Current Neurology and Neuroscience Reports / Issue 3/2017
Print ISSN: 1528-4042
Electronic ISSN: 1534-6293
DOI
https://doi.org/10.1007/s11910-017-0735-0

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