Skip to main content
Top
Published in: Neuropsychology Review 4/2014

01-12-2014 | Review

Understanding the Neuropsychiatric Phenotype of Fragile X-Associated Tremor Ataxia Syndrome: a Systematic Review

Authors: R. C. Birch, K. M. Cornish, D. R. Hocking, J. N. Trollor

Published in: Neuropsychology Review | Issue 4/2014

Login to get access

Abstract

Fragile X-associated tremor ataxia syndrome (FXTAS) is a recently identified X-linked neurodegenerative disorder affecting a proportion of premutation carriers of the Fragile X Mental Retardation 1 (FMR1) gene. Previous research suggests that cognitive and psychiatric features of FXTAS may include primary impairments in executive function and increased vulnerability to mood and anxiety disorders. A number of these reports, however, are based on overlapping cohorts or have produced inconsistent findings. A systematic review was therefore conducted to further elucidate the neuropsychiatric features characteristic of FXTAS. Fourteen papers met inclusion criteria for the review and were considered to represent nine independent FXTAS cohorts. Findings from the review suggest that the neuropsychiatric phenotype of FXTAS is characterised primarily by poorer performance on measures of executive function, working memory, information processing speed, and fine motor control when compared to matched comparison groups. Two studies were identified in which psychiatric symptoms in FXTAS were compared with controls, and these yielded mixed results. Overall the results of this review support previous reports that the neuropsychiatric profile of FXTAS is consistent with a dysexecutive fronto-subcortical syndrome. However, additional controlled studies are required to progress our understanding of FXTAS and how the neuropsychiatric profile relates to underlying pathological mechanisms.
Literature
go back to reference Adams, J. S., Adams, P. E., Nguyen, D., Brunberg, J. A., Tassone, F., Zhang, W., et al. (2007). Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS). Neurology, 69(9), 851–859.PubMedCrossRef Adams, J. S., Adams, P. E., Nguyen, D., Brunberg, J. A., Tassone, F., Zhang, W., et al. (2007). Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS). Neurology, 69(9), 851–859.PubMedCrossRef
go back to reference Adams, P. E., Adams, J. S., Nguyen, D. V., Hessl, D., Brunberg, J. A., Tassone, F., et al. (2010). Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 153B(3), 775–785. Adams, P. E., Adams, J. S., Nguyen, D. V., Hessl, D., Brunberg, J. A., Tassone, F., et al. (2010). Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 153B(3), 775–785.
go back to reference Alexander, G. E., & Crutcher, M. D. (1990). Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends in Neurosciences, 13(7), 266–271.PubMedCrossRef Alexander, G. E., & Crutcher, M. D. (1990). Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends in Neurosciences, 13(7), 266–271.PubMedCrossRef
go back to reference Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986). Parallel organization of functionally segregated circuits linking Basal Ganglia and Cortex. Annual Review of Neuroscience, 9(1), 357–381.PubMedCrossRef Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986). Parallel organization of functionally segregated circuits linking Basal Ganglia and Cortex. Annual Review of Neuroscience, 9(1), 357–381.PubMedCrossRef
go back to reference Allen, E. G., Hunter, J. E., Rusin, M., Juncos, J., Novak, G., Hamilton, D., et al. (2011). Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome. Neuropsychology, 25(3), 404–411.PubMedCentralPubMedCrossRef Allen, E. G., Hunter, J. E., Rusin, M., Juncos, J., Novak, G., Hamilton, D., et al. (2011). Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome. Neuropsychology, 25(3), 404–411.PubMedCentralPubMedCrossRef
go back to reference American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5th ed.). Arlington: American Psychiatric Association. American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5th ed.). Arlington: American Psychiatric Association.
go back to reference Amiri, K., Hagerman, R. J., & Hagerman, P. J. (2008). Fragile X-associated tremor/ataxia syndrome—an aging face of the fragile X gene. Archives of Neurology, 65(1), 19–25.PubMedCrossRef Amiri, K., Hagerman, R. J., & Hagerman, P. J. (2008). Fragile X-associated tremor/ataxia syndrome—an aging face of the fragile X gene. Archives of Neurology, 65(1), 19–25.PubMedCrossRef
go back to reference Apartis, E., Blancher, A., Meissner, W. G., Guyant-Marechal, L., Maltete, D., De Broucker, T., et al. (2012). FXTAS: new insights and the need for revised diagnostic criteria. Neurology, 79(18), 1898–1907.PubMedCrossRef Apartis, E., Blancher, A., Meissner, W. G., Guyant-Marechal, L., Maltete, D., De Broucker, T., et al. (2012). FXTAS: new insights and the need for revised diagnostic criteria. Neurology, 79(18), 1898–1907.PubMedCrossRef
go back to reference Bacalman, S., Farzin, F., Bourgeois, J. A., Cogswell, J., Goodlin-Jones, B. L., Gane, L. W., et al. (2006). Psychiatric phenotype of the fragile X-associated tremor/ataxia syndrome (FXTAS) in males: newly described fronto-subcortical dementia. Journal of Clinical Psychiatry, 67(1), 87–94.PubMedCrossRef Bacalman, S., Farzin, F., Bourgeois, J. A., Cogswell, J., Goodlin-Jones, B. L., Gane, L. W., et al. (2006). Psychiatric phenotype of the fragile X-associated tremor/ataxia syndrome (FXTAS) in males: newly described fronto-subcortical dementia. Journal of Clinical Psychiatry, 67(1), 87–94.PubMedCrossRef
go back to reference Bernard, J. A., Seidler, R. D., Hassevoort, K. M., Benson, B. L., Welsh, R. C., Wiggins, J. L., et al. (2012). Resting state cortico-cerebellar functional connectivity networks: a comparison of anatomical and self-organizing map approached. Frontiers in Neuroanatomy, 6, 31–50.PubMedCentralPubMedCrossRef Bernard, J. A., Seidler, R. D., Hassevoort, K. M., Benson, B. L., Welsh, R. C., Wiggins, J. L., et al. (2012). Resting state cortico-cerebellar functional connectivity networks: a comparison of anatomical and self-organizing map approached. Frontiers in Neuroanatomy, 6, 31–50.PubMedCentralPubMedCrossRef
go back to reference Bernard, J. A., Peltier, S. J., Wiggins, J. L., Jaeggi, S. M., Buschkuehl, M., Fling, B. W., et al. (2013). Disrupted cortico-cerebellar connectivity in older adults. NeuroImage, 83, 103–119.PubMedCrossRef Bernard, J. A., Peltier, S. J., Wiggins, J. L., Jaeggi, S. M., Buschkuehl, M., Fling, B. W., et al. (2013). Disrupted cortico-cerebellar connectivity in older adults. NeuroImage, 83, 103–119.PubMedCrossRef
go back to reference Berry-Kravis, E., Potanos, K., Weinberg, D., Zhou, L. L., & Goetz, C. G. (2005). Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation. Annals of Neurology, 57(1), 144–147.PubMedCrossRef Berry-Kravis, E., Potanos, K., Weinberg, D., Zhou, L. L., & Goetz, C. G. (2005). Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation. Annals of Neurology, 57(1), 144–147.PubMedCrossRef
go back to reference Berry-Kravis, E., Goetz, C. G., Leehey, M. A., Hagerman, R. J., Zhang, L., Li, L. X., et al. (2007). Neuropathic features in fragile X premutation carriers. American Journal of Medical Genetics Part A, 143A(1), 19–26.PubMedCrossRef Berry-Kravis, E., Goetz, C. G., Leehey, M. A., Hagerman, R. J., Zhang, L., Li, L. X., et al. (2007). Neuropathic features in fragile X premutation carriers. American Journal of Medical Genetics Part A, 143A(1), 19–26.PubMedCrossRef
go back to reference Biancalana, V., Toft, M., Le Ber, I., Tison, F., Scherrer, E., Thibodeau, S., et al. (2005). FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy. Archives of Neurology, 62(6), 962–966.PubMedCrossRef Biancalana, V., Toft, M., Le Ber, I., Tison, F., Scherrer, E., Thibodeau, S., et al. (2005). FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy. Archives of Neurology, 62(6), 962–966.PubMedCrossRef
go back to reference Bodden, M. E., Mollenhauer, B., Trenkwalder, C., Cabanel, N., Eggert, K. M., Unger, M. M., et al. (2010). Affective and cognitive theory of mind in patients with Parkinson’s Disease. Parkinsonism & Related Disorders, 16(7), 466–470.CrossRef Bodden, M. E., Mollenhauer, B., Trenkwalder, C., Cabanel, N., Eggert, K. M., Unger, M. M., et al. (2010). Affective and cognitive theory of mind in patients with Parkinson’s Disease. Parkinsonism & Related Disorders, 16(7), 466–470.CrossRef
go back to reference Bourgeois, J. A., Cogswell, J. B., Hessl, D., Zhang, L., Ono, M. Y., Tassone, F., et al. (2007). Cognitive, anxiety and mood disorders in the fragile X-associated tremor/ataxia syndrome. General Hospital Psychiatry, 29(4), 349–356.PubMedCentralPubMedCrossRef Bourgeois, J. A., Cogswell, J. B., Hessl, D., Zhang, L., Ono, M. Y., Tassone, F., et al. (2007). Cognitive, anxiety and mood disorders in the fragile X-associated tremor/ataxia syndrome. General Hospital Psychiatry, 29(4), 349–356.PubMedCentralPubMedCrossRef
go back to reference Bourgeois, J. A., Coffey, S. M., Rivera, S. M., Hessl, D., Gane, L. W., Tassone, F., et al. (2009). A review of fragile X premutation disorders: expanding the psychiatric perspective. Journal of Clinical Psychiatry, 70(6), 852–862.PubMedCentralPubMedCrossRef Bourgeois, J. A., Coffey, S. M., Rivera, S. M., Hessl, D., Gane, L. W., Tassone, F., et al. (2009). A review of fragile X premutation disorders: expanding the psychiatric perspective. Journal of Clinical Psychiatry, 70(6), 852–862.PubMedCentralPubMedCrossRef
go back to reference Bourgeois, J. A., Seritan, A. L., Casillas, M., Hessl, D., Schneider, A., Yang, Y., et al. (2011). Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers. The Journal of Clinical Psychiatry, 72(2), 175–182.PubMedCentralPubMedCrossRef Bourgeois, J. A., Seritan, A. L., Casillas, M., Hessl, D., Schneider, A., Yang, Y., et al. (2011). Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers. The Journal of Clinical Psychiatry, 72(2), 175–182.PubMedCentralPubMedCrossRef
go back to reference Brega, A. G., Goodrich, G., Bennett, R. E., Hessl, D., Engle, K., Leehey, M. A., et al. (2008). The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome. Journal of Clinical and Experimental Neuropsychology, 30(8), 853–869.PubMedCentralPubMedCrossRef Brega, A. G., Goodrich, G., Bennett, R. E., Hessl, D., Engle, K., Leehey, M. A., et al. (2008). The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome. Journal of Clinical and Experimental Neuropsychology, 30(8), 853–869.PubMedCentralPubMedCrossRef
go back to reference Brega, A. G., Reynolds, A., Bennett, R. E., Leehey, M. A., Bounds, L. S., Cogswell, J. B., et al. (2009). Functional status of men with the fragile X premutation, with and without the tremor/ataxia syndrome (FXTAS). International Journal of Geriatric Psychiatry, 24(10), 1101–1109.PubMedCrossRef Brega, A. G., Reynolds, A., Bennett, R. E., Leehey, M. A., Bounds, L. S., Cogswell, J. B., et al. (2009). Functional status of men with the fragile X premutation, with and without the tremor/ataxia syndrome (FXTAS). International Journal of Geriatric Psychiatry, 24(10), 1101–1109.PubMedCrossRef
go back to reference Brunberg, J. A., Jacquemont, S., Hagerman, R. J., Berry-Kravis, E. M., Grigsby, J., Leehey, M. A., et al. (2002). Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction. American Journal of Neuroradiology, 23(10), 1757–1766.PubMed Brunberg, J. A., Jacquemont, S., Hagerman, R. J., Berry-Kravis, E. M., Grigsby, J., Leehey, M. A., et al. (2002). Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction. American Journal of Neuroradiology, 23(10), 1757–1766.PubMed
go back to reference Bürk, K., Daum, I., & Rüb, U. (2006). Cognitive function in multiple system atrophy of the cerebellar type. Movement Disorders, 21(6), 772–776.PubMedCrossRef Bürk, K., Daum, I., & Rüb, U. (2006). Cognitive function in multiple system atrophy of the cerebellar type. Movement Disorders, 21(6), 772–776.PubMedCrossRef
go back to reference Capelli, L. P., Goncalves, M. R., Leite, C. C., Barbosa, E. R., Nitrini, R., Vianna-Morgante, A. M., et al. (2010). The fragile x-associated tremor and ataxia syndrome (FXTAS). Arquivos de Neuro-Psiquiatria, 68(5), 791–798.PubMedCrossRef Capelli, L. P., Goncalves, M. R., Leite, C. C., Barbosa, E. R., Nitrini, R., Vianna-Morgante, A. M., et al. (2010). The fragile x-associated tremor and ataxia syndrome (FXTAS). Arquivos de Neuro-Psiquiatria, 68(5), 791–798.PubMedCrossRef
go back to reference Chonchaiya, W., Nguyen, D. V., Au, J., Campos, L., Berry-Kravis, E. M., Lohse, K., et al. (2010). Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome. Clinical Genetics, 78(1), 38–46.PubMedCentralPubMedCrossRef Chonchaiya, W., Nguyen, D. V., Au, J., Campos, L., Berry-Kravis, E. M., Lohse, K., et al. (2010). Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome. Clinical Genetics, 78(1), 38–46.PubMedCentralPubMedCrossRef
go back to reference Cohen, S., Masyn, K., Adams, J., Hessl, D., Rivera, S., Tassone, F., et al. (2006). Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome. Neurology, 67(8), 1426–1431.PubMedCrossRef Cohen, S., Masyn, K., Adams, J., Hessl, D., Rivera, S., Tassone, F., et al. (2006). Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome. Neurology, 67(8), 1426–1431.PubMedCrossRef
go back to reference Cornish, K., Kogan, C., Turk, J., Manly, T., James, N., Mills, A., et al. (2005). The emerging fragile X premutation phenotype: evidence from the domain of social cognition. Brain and Cognition, 57(1), 53–60.PubMedCrossRef Cornish, K., Kogan, C., Turk, J., Manly, T., James, N., Mills, A., et al. (2005). The emerging fragile X premutation phenotype: evidence from the domain of social cognition. Brain and Cognition, 57(1), 53–60.PubMedCrossRef
go back to reference Cornish, K. M., Li, L., Kogan, C. S., Jacquemont, S., Turk, J., Dalton, A., et al. (2008). Age-dependent cognitive changes in carriers of the fragile X syndrome. Cortex, 44(6), 628–636.PubMedCrossRef Cornish, K. M., Li, L., Kogan, C. S., Jacquemont, S., Turk, J., Dalton, A., et al. (2008). Age-dependent cognitive changes in carriers of the fragile X syndrome. Cortex, 44(6), 628–636.PubMedCrossRef
go back to reference Cornish, K. M., Kogan, C. S., Li, L. X., Turk, J., Jacquemont, S., & Hagerman, R. J. (2009). Lifespan changes in working memory in fragile X premutation males. Brain and Cognition, 69(3), 551–558.PubMedCentralPubMedCrossRef Cornish, K. M., Kogan, C. S., Li, L. X., Turk, J., Jacquemont, S., & Hagerman, R. J. (2009). Lifespan changes in working memory in fragile X premutation males. Brain and Cognition, 69(3), 551–558.PubMedCentralPubMedCrossRef
go back to reference Cornish, K. M., Hocking, D. R., Moss, S. A., & Kogan, C. S. (2011). Selective executive markers of at-risk profiles associated with the fragile X premutation. Neurology, 77(7), 618–622.PubMedCentralPubMedCrossRef Cornish, K. M., Hocking, D. R., Moss, S. A., & Kogan, C. S. (2011). Selective executive markers of at-risk profiles associated with the fragile X premutation. Neurology, 77(7), 618–622.PubMedCentralPubMedCrossRef
go back to reference Duff, K., Paulsen, J. S., Beglinger, L. J., Langbehn, D. R., & Stout, J. C. (2007). Psychiatric symptoms in Huntington’s disease before diagnosis: the predict-HD study. Biological Psychiatry, 62(12), 1341–1346.PubMedCrossRef Duff, K., Paulsen, J. S., Beglinger, L. J., Langbehn, D. R., & Stout, J. C. (2007). Psychiatric symptoms in Huntington’s disease before diagnosis: the predict-HD study. Biological Psychiatry, 62(12), 1341–1346.PubMedCrossRef
go back to reference Duff, K., Paulsen, J. S., Beglinger, L. J., Langbehn, D. R., Wang, C., Stout, J. C., et al. (2010). “Frontal” behaviors before the diagnosis of Huntington’s disease and its relationship to markers of disease progression: evidence of early lack of awareness. Journal of Neuropsychiatry and Clinical Neurosciences, 22(2), 196–207.PubMedCentralPubMedCrossRef Duff, K., Paulsen, J. S., Beglinger, L. J., Langbehn, D. R., Wang, C., Stout, J. C., et al. (2010). “Frontal” behaviors before the diagnosis of Huntington’s disease and its relationship to markers of disease progression: evidence of early lack of awareness. Journal of Neuropsychiatry and Clinical Neurosciences, 22(2), 196–207.PubMedCentralPubMedCrossRef
go back to reference Fahn, S., Tolosa, E., & Marin, C. (1993). Clinical rating scale for tremor. In J. Jankovic & E. Tolosa (Eds.), Parkinson’s Disease and movement disorders (pp. 271–280). Baltimore: Williams and Wilkins. Fahn, S., Tolosa, E., & Marin, C. (1993). Clinical rating scale for tremor. In J. Jankovic & E. Tolosa (Eds.), Parkinson’s Disease and movement disorders (pp. 271–280). Baltimore: Williams and Wilkins.
go back to reference Ghosh, B. C., Calder, A. J., Peers, P. V., Lawrence, A. D., Acosta-Cabronero, J., Pereira, J. M., et al. (2012). Social cognitive deficits and their neural correlates in progressive supranuclear palsy. Brain, 135(Pt 7), 2089–2102.PubMedCentralPubMedCrossRef Ghosh, B. C., Calder, A. J., Peers, P. V., Lawrence, A. D., Acosta-Cabronero, J., Pereira, J. M., et al. (2012). Social cognitive deficits and their neural correlates in progressive supranuclear palsy. Brain, 135(Pt 7), 2089–2102.PubMedCentralPubMedCrossRef
go back to reference Greco, C. M., Hagerman, R. J., Tassone, F., Chudley, A. E., Del Bigio, M. R., Jacquemont, S., et al. (2002). Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain, 125, 1760–1771.PubMedCrossRef Greco, C. M., Hagerman, R. J., Tassone, F., Chudley, A. E., Del Bigio, M. R., Jacquemont, S., et al. (2002). Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain, 125, 1760–1771.PubMedCrossRef
go back to reference Greco, C. M., Tassone, F., Garcia-Arocena, D., Tartaglia, N., Coffey, S. M., Vartanian, T. K., et al. (2008). Clinical and neuropathologic findings in a woman with the FMR1 premutation and multiple sclerosis. Archives of Neurology, 65(8), 1114–1116.PubMedCentralPubMedCrossRef Greco, C. M., Tassone, F., Garcia-Arocena, D., Tartaglia, N., Coffey, S. M., Vartanian, T. K., et al. (2008). Clinical and neuropathologic findings in a woman with the FMR1 premutation and multiple sclerosis. Archives of Neurology, 65(8), 1114–1116.PubMedCentralPubMedCrossRef
go back to reference Grigsby, J., Brega, A. G., Jacquemont, S., Loesch, D. Z., Leehey, M. A., Goodrich, G. K., et al. (2006). Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of the Neurological Sciences, 248(1–2), 227–233.PubMedCrossRef Grigsby, J., Brega, A. G., Jacquemont, S., Loesch, D. Z., Leehey, M. A., Goodrich, G. K., et al. (2006). Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of the Neurological Sciences, 248(1–2), 227–233.PubMedCrossRef
go back to reference Grigsby, J., Brega, A. G., Leehey, M. A., Goodrich, G. K., Jacquemont, S., Loesch, D. Z., et al. (2007). Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome. Movement Disorders, 22(5), 645–650.PubMedCrossRef Grigsby, J., Brega, A. G., Leehey, M. A., Goodrich, G. K., Jacquemont, S., Loesch, D. Z., et al. (2007). Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome. Movement Disorders, 22(5), 645–650.PubMedCrossRef
go back to reference Grigsby, J., Brega, A. G., Engle, K., Leehey, M. A., Hagerman, R. J., Tassone, F., et al. (2008). Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome. Neuropsychology, 22(1), 48–60.PubMedCrossRef Grigsby, J., Brega, A. G., Engle, K., Leehey, M. A., Hagerman, R. J., Tassone, F., et al. (2008). Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome. Neuropsychology, 22(1), 48–60.PubMedCrossRef
go back to reference Hagerman, P. J., & Hagerman, R. J. (2004b). Fragile X-associated tremor/ataxia syndrome (FXTAS). Mental Retardation and Developmental Disabilities Research Reviews, 10(1), 25–30.PubMedCrossRef Hagerman, P. J., & Hagerman, R. J. (2004b). Fragile X-associated tremor/ataxia syndrome (FXTAS). Mental Retardation and Developmental Disabilities Research Reviews, 10(1), 25–30.PubMedCrossRef
go back to reference Hagerman, R., & Hagerman, P. (2013). Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome. Lancet Neurology, 12(8), 786–798.PubMedCentralCrossRef Hagerman, R., & Hagerman, P. (2013). Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome. Lancet Neurology, 12(8), 786–798.PubMedCentralCrossRef
go back to reference Hagerman, R. J., Leehey, M., Heinrichs, W., Tassone, F., Wilson, R., Hills, J., et al. (2001). Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology, 57(1), 127–130.PubMedCrossRef Hagerman, R. J., Leehey, M., Heinrichs, W., Tassone, F., Wilson, R., Hills, J., et al. (2001). Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology, 57(1), 127–130.PubMedCrossRef
go back to reference Hagerman, R. J., Leavitt, B. R., Farzin, F., Jacquemont, S., Greco, C. M., Brunberg, J. A., et al. (2004). Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. American Journal of Human Genetics, 74(5), 1051–1056.PubMedCentralPubMedCrossRef Hagerman, R. J., Leavitt, B. R., Farzin, F., Jacquemont, S., Greco, C. M., Brunberg, J. A., et al. (2004). Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. American Journal of Human Genetics, 74(5), 1051–1056.PubMedCentralPubMedCrossRef
go back to reference Hall, D. A., Berry-Kravis, E., Zhang, W., Tassone, F., Spector, E., Zerbe, G., et al. (2011). FMR1 gray-zone alleles: association with Parkinson’s Disease in women? Movement Disorders, 26(10), 1900–1906.PubMedCentralPubMedCrossRef Hall, D. A., Berry-Kravis, E., Zhang, W., Tassone, F., Spector, E., Zerbe, G., et al. (2011). FMR1 gray-zone alleles: association with Parkinson’s Disease in women? Movement Disorders, 26(10), 1900–1906.PubMedCentralPubMedCrossRef
go back to reference Hall, D., Tassone, F., Klepitskaya, O., & Leehey, M. (2012). Fragile X–associated tremor ataxia syndrome in FMR1 gray zone allele carriers. Movement Disorders, 27(2), 297–301.CrossRef Hall, D., Tassone, F., Klepitskaya, O., & Leehey, M. (2012). Fragile X–associated tremor ataxia syndrome in FMR1 gray zone allele carriers. Movement Disorders, 27(2), 297–301.CrossRef
go back to reference Hashimoto, R., Backer, K. C., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2011a). An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of Psychiatric Research, 45(1), 36–43.PubMedCentralPubMedCrossRef Hashimoto, R., Backer, K. C., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2011a). An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of Psychiatric Research, 45(1), 36–43.PubMedCentralPubMedCrossRef
go back to reference Hashimoto, R., Javan, A. K., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2011b). A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome. Brain, 134(3), 863–878. Hashimoto, R., Javan, A. K., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2011b). A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome. Brain, 134(3), 863–878.
go back to reference Hashimoto, R., Srivastava, S., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2011c). Diffusion tensor imaging in male premutation carriers of the fragile x mental retardation gene. Movement Disorders, 26(7), 1329–1336.PubMedCentralPubMedCrossRef Hashimoto, R., Srivastava, S., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2011c). Diffusion tensor imaging in male premutation carriers of the fragile x mental retardation gene. Movement Disorders, 26(7), 1329–1336.PubMedCentralPubMedCrossRef
go back to reference Hessl, D., Tassone, F., Loesch, D. Z., Berry-Kravis, E., Leehey, M. A., Gane, L. W., et al. (2005). Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 139B(1), 115–121.CrossRef Hessl, D., Tassone, F., Loesch, D. Z., Berry-Kravis, E., Leehey, M. A., Gane, L. W., et al. (2005). Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 139B(1), 115–121.CrossRef
go back to reference Hessl, D., Rivera, S., Koldewyn, K., Cordeiro, L., Adams, J., Tassone, F., et al. (2007). Amygdala dysfunction in men with the fragile X premutation. Brain, 130, 404–416.PubMedCrossRef Hessl, D., Rivera, S., Koldewyn, K., Cordeiro, L., Adams, J., Tassone, F., et al. (2007). Amygdala dysfunction in men with the fragile X premutation. Brain, 130, 404–416.PubMedCrossRef
go back to reference Hessl, D., Wang, J. M., Schneider, A., Koldewyn, K., Le, L., Iwahashi, C., et al. (2011). Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation. Biological Psychiatry, 70(9), 859–865.PubMedCentralPubMedCrossRef Hessl, D., Wang, J. M., Schneider, A., Koldewyn, K., Le, L., Iwahashi, C., et al. (2011). Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation. Biological Psychiatry, 70(9), 859–865.PubMedCentralPubMedCrossRef
go back to reference Higginson, C. I., King, D. S., Levine, D., Wheelock, V. L., Khamphay, N. O., & Sigvardt, K. A. (2003). The relationship between executive function and verbal memory in Parkinson’s Disease. Brain and Cognition, 52(3), 343–352.PubMedCrossRef Higginson, C. I., King, D. S., Levine, D., Wheelock, V. L., Khamphay, N. O., & Sigvardt, K. A. (2003). The relationship between executive function and verbal memory in Parkinson’s Disease. Brain and Cognition, 52(3), 343–352.PubMedCrossRef
go back to reference Hocking, D. R., Kogan, C. S., & Cornish, K. M. (2012a). Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation. Brain and Cognition, 79, 39–44.PubMedCrossRef Hocking, D. R., Kogan, C. S., & Cornish, K. M. (2012a). Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation. Brain and Cognition, 79, 39–44.PubMedCrossRef
go back to reference Hocking, D. R., Kogan, C. S., & Cornish, K. M. (2012b). Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation. Brain & Cognition, 79(1), 39–44.CrossRef Hocking, D. R., Kogan, C. S., & Cornish, K. M. (2012b). Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation. Brain & Cognition, 79(1), 39–44.CrossRef
go back to reference Horvath, J., Burkhard, P. R., Morris, M., Bottani, A., Moix, I., & Delavelle, J. (2007). Expanding the phenotype of fragile x-associated tremor/ataxia syndrome: A new female case. Movement Disorders, 22(11). Horvath, J., Burkhard, P. R., Morris, M., Bottani, A., Moix, I., & Delavelle, J. (2007). Expanding the phenotype of fragile x-associated tremor/ataxia syndrome: A new female case. Movement Disorders, 22(11).
go back to reference Hunter, J. E., Abramowitz, A., Rusin, M., & Sherman, S. L. (2009). Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature. Genetics in Medicine, 11(2), 79–89.PubMedCentralPubMedCrossRef Hunter, J. E., Abramowitz, A., Rusin, M., & Sherman, S. L. (2009). Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature. Genetics in Medicine, 11(2), 79–89.PubMedCentralPubMedCrossRef
go back to reference Hunter, J. E., Sherman, S., Grigsby, J., Kogan, C., & Cornish, K. (2012). Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology, 26(2), 156–164.PubMedCentralPubMedCrossRef Hunter, J. E., Sherman, S., Grigsby, J., Kogan, C., & Cornish, K. (2012). Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology, 26(2), 156–164.PubMedCentralPubMedCrossRef
go back to reference Jacquemont, S., Hagerman, R. J., Leehey, M., Grigsby, J., Zhang, L., Brunberg, J. A., et al. (2003). Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. The American Journal of Human Genetics, 72(4), 869–878.CrossRef Jacquemont, S., Hagerman, R. J., Leehey, M., Grigsby, J., Zhang, L., Brunberg, J. A., et al. (2003). Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. The American Journal of Human Genetics, 72(4), 869–878.CrossRef
go back to reference Jacquemont, S., Orrico, A., Galli, L., Sahota, P. K., Brunberg, J. A., Anichini, C., et al. (2005). Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS? Journal of Medical Genetics, 42(2), e14.PubMedCentralPubMedCrossRef Jacquemont, S., Orrico, A., Galli, L., Sahota, P. K., Brunberg, J. A., Anichini, C., et al. (2005). Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS? Journal of Medical Genetics, 42(2), e14.PubMedCentralPubMedCrossRef
go back to reference Johnston, C., Eliez, S., Dyer-Friedman, J., Hessl, D., Glaser, B., Blasey, C., et al. (2001). Neurobehavioral phenotype in carriers of the fragile X premutation. American Journal of Medical Genetics, 103(4), 314–319.PubMedCrossRef Johnston, C., Eliez, S., Dyer-Friedman, J., Hessl, D., Glaser, B., Blasey, C., et al. (2001). Neurobehavioral phenotype in carriers of the fragile X premutation. American Journal of Medical Genetics, 103(4), 314–319.PubMedCrossRef
go back to reference Juncos, J., Lazarus, J., Graves-Allen, E., Shubeck, L., Rusin, M., Novak, G., et al. (2011). New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS). Neurogenetics, 12(2), 123–135.PubMedCentralPubMedCrossRef Juncos, J., Lazarus, J., Graves-Allen, E., Shubeck, L., Rusin, M., Novak, G., et al. (2011). New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS). Neurogenetics, 12(2), 123–135.PubMedCentralPubMedCrossRef
go back to reference Karmon, Y., & Gadoth, N. (2008). Fragile X associated tremor/ataxia syndrome (FXTAS) with dementia in a female harbouring FMR1 premutation. Journal of Neurology, Neurosurgery and Psychiatry, 79(6), 738–739.PubMedCrossRef Karmon, Y., & Gadoth, N. (2008). Fragile X associated tremor/ataxia syndrome (FXTAS) with dementia in a female harbouring FMR1 premutation. Journal of Neurology, Neurosurgery and Psychiatry, 79(6), 738–739.PubMedCrossRef
go back to reference Kenneson, A., Zhang, F., Hagedorn, C. H., & Warren, S. T. (2001). Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers. Human Molecular Genetics, 10(14), 1449–1454.PubMedCrossRef Kenneson, A., Zhang, F., Hagedorn, C. H., & Warren, S. T. (2001). Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers. Human Molecular Genetics, 10(14), 1449–1454.PubMedCrossRef
go back to reference Kogan, C. S., & Cornish, K. M. (2010). Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS. Brain and Cognition, 73(3), 236–243.PubMedCrossRef Kogan, C. S., & Cornish, K. M. (2010). Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS. Brain and Cognition, 73(3), 236–243.PubMedCrossRef
go back to reference Kurz, M. W., Schlitter, M. A., Klenk, Y., Mueller, T., Larsen, J. P., Aarsland, D., et al. (2007). FMR1 alleles in Parkinson’s Disease: relation to cognitive decline and hallucinations, a longitudinal study. Journal of Geriatric Psychiatry and Neurology, 20(2), 89–92.PubMedCrossRef Kurz, M. W., Schlitter, M. A., Klenk, Y., Mueller, T., Larsen, J. P., Aarsland, D., et al. (2007). FMR1 alleles in Parkinson’s Disease: relation to cognitive decline and hallucinations, a longitudinal study. Journal of Geriatric Psychiatry and Neurology, 20(2), 89–92.PubMedCrossRef
go back to reference Lezak, M. D., Howieson, D. B., & Loring, D. W. (2004). Neuropsychological assessment (Vol. 4). Oxford: Oxford University Press. Lezak, M. D., Howieson, D. B., & Loring, D. W. (2004). Neuropsychological assessment (Vol. 4). Oxford: Oxford University Press.
go back to reference Loesch, D. Z., Churchyard, A., Brotchie, P., Marot, M., & Tassone, F. (2005). Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond. Clinical Genetics, 67(5), 412–417.PubMedCrossRef Loesch, D. Z., Churchyard, A., Brotchie, P., Marot, M., & Tassone, F. (2005). Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond. Clinical Genetics, 67(5), 412–417.PubMedCrossRef
go back to reference Loesch, D. Z., Bui, Q. M., Huggins, R. M., Mitchell, R. J., Hagerman, R. J., & Tassone, F. (2007). Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats. Journal of Medical Genetics, 44(3), 200–204.PubMedCentralPubMedCrossRef Loesch, D. Z., Bui, Q. M., Huggins, R. M., Mitchell, R. J., Hagerman, R. J., & Tassone, F. (2007). Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats. Journal of Medical Genetics, 44(3), 200–204.PubMedCentralPubMedCrossRef
go back to reference Loesch, D. Z., Khaniani, M. S., Slater, H. R., Rubio, J. P., Bui, Q. M., Kotschet, K., et al. (2009). Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism. Clinical Genetics, 76(5). Loesch, D. Z., Khaniani, M. S., Slater, H. R., Rubio, J. P., Bui, Q. M., Kotschet, K., et al. (2009). Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism. Clinical Genetics, 76(5).
go back to reference Middleton, F. A., & Strick, P. L. (2000). Basal ganglia and cerebellar loops: motor and cognitive circuits. Brain Research Reviews, 31(2–3), 236–250.PubMedCrossRef Middleton, F. A., & Strick, P. L. (2000). Basal ganglia and cerebellar loops: motor and cognitive circuits. Brain Research Reviews, 31(2–3), 236–250.PubMedCrossRef
go back to reference Mothersead, P. K., Conrad, K., Hagerman, R. J., Greco, C. M., Hessl, D., & Tassone, F. (2005). An atypical progressive dementia in a male carrier of the fragile X premutation: an example of fragile X-associated tremor/ataxia syndrome. Applied Neuropsychology, 12(3), 169–178.PubMedCrossRef Mothersead, P. K., Conrad, K., Hagerman, R. J., Greco, C. M., Hessl, D., & Tassone, F. (2005). An atypical progressive dementia in a male carrier of the fragile X premutation: an example of fragile X-associated tremor/ataxia syndrome. Applied Neuropsychology, 12(3), 169–178.PubMedCrossRef
go back to reference Olichney, J. M., Chan, S. H., Wong, L. M., Schneider, A., Seritan, A., Niese, A., et al. (2010). Abnormal N400 word repetition effects in fragile X-associated tremor/ataxia syndrome. Brain, 133, 1438–1450.PubMedCentralPubMedCrossRef Olichney, J. M., Chan, S. H., Wong, L. M., Schneider, A., Seritan, A., Niese, A., et al. (2010). Abnormal N400 word repetition effects in fragile X-associated tremor/ataxia syndrome. Brain, 133, 1438–1450.PubMedCentralPubMedCrossRef
go back to reference Reis, A. H. O., Ferreira, A. C. S., Gomes, K. B., Aguiar, M. J. B., Fonseca, C. G., Cardoso, F. E., et al. (2008). Frequency of FMR1 premutation in individuals with ataxia and/or tremor and/or parkinsonism. Genetics and Molecular Research, 7(1), 74–84.PubMedCrossRef Reis, A. H. O., Ferreira, A. C. S., Gomes, K. B., Aguiar, M. J. B., Fonseca, C. G., Cardoso, F. E., et al. (2008). Frequency of FMR1 premutation in individuals with ataxia and/or tremor and/or parkinsonism. Genetics and Molecular Research, 7(1), 74–84.PubMedCrossRef
go back to reference Roca, M., Torralva, T., Meli, F., Fiol, M., Calcagno, M., Carpintiero, S., et al. (2008). Cognitive deficits in multiple sclerosis correlate with changes in fronto-subcortical tracts. Multiple Sclerosis, 14(3), 364–369.PubMedCrossRef Roca, M., Torralva, T., Meli, F., Fiol, M., Calcagno, M., Carpintiero, S., et al. (2008). Cognitive deficits in multiple sclerosis correlate with changes in fronto-subcortical tracts. Multiple Sclerosis, 14(3), 364–369.PubMedCrossRef
go back to reference Roca, M., Torralva, T., Gleichgerrcht, E., Chade, A., Arevalo, G. G., Gershanik, O., et al. (2010). Impairments in social cognition in early medicated and unmedicated Parkinson disease. Cognitive & Behavioral Neurology, 23(3), 152–158.CrossRef Roca, M., Torralva, T., Gleichgerrcht, E., Chade, A., Arevalo, G. G., Gershanik, O., et al. (2010). Impairments in social cognition in early medicated and unmedicated Parkinson disease. Cognitive & Behavioral Neurology, 23(3), 152–158.CrossRef
go back to reference Rodriguez-Revenga, L., Madrigal, I., Pagonabarraga, J., Xuncla, M., Badenas, C., Kulisevsky, J., et al. (2009). Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families. European Journal of Human Genetics, 17(10), 1359–1362.PubMedCentralPubMedCrossRef Rodriguez-Revenga, L., Madrigal, I., Pagonabarraga, J., Xuncla, M., Badenas, C., Kulisevsky, J., et al. (2009). Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families. European Journal of Human Genetics, 17(10), 1359–1362.PubMedCentralPubMedCrossRef
go back to reference Rodriguez-Revenga, L., Pagonabarraga, J., Gomez-Anson, B., Lopez-Mourelo, O., Madrigal, I., Xuncla, M., et al. (2010). Motor and mental dysfunction in mother-daughter transmitted FXTAS. Neurology, 75(15), 1370–1376.PubMedCrossRef Rodriguez-Revenga, L., Pagonabarraga, J., Gomez-Anson, B., Lopez-Mourelo, O., Madrigal, I., Xuncla, M., et al. (2010). Motor and mental dysfunction in mother-daughter transmitted FXTAS. Neurology, 75(15), 1370–1376.PubMedCrossRef
go back to reference Rosas, H. D., Salat, D. H., Lee, S. Y., Zaleta, A. K., Pappu, V., Fischl, B., et al. (2008). Cerebral cortex and the clinical expression of Huntington’s disease: complexity and heterogeneity. Brain, 131(4), 1057–1068.PubMedCentralPubMedCrossRef Rosas, H. D., Salat, D. H., Lee, S. Y., Zaleta, A. K., Pappu, V., Fischl, B., et al. (2008). Cerebral cortex and the clinical expression of Huntington’s disease: complexity and heterogeneity. Brain, 131(4), 1057–1068.PubMedCentralPubMedCrossRef
go back to reference Santangelo, G., Vitale, C., Trojano, L., Errico, D., Amboni, M., Barbarulo, A. M., et al. (2012). Neuropsychological correlates of theory of mind in patients with early Parkinson’s Disease. Movement Disorders, 27(1), 98–105.PubMedCrossRef Santangelo, G., Vitale, C., Trojano, L., Errico, D., Amboni, M., Barbarulo, A. M., et al. (2012). Neuropsychological correlates of theory of mind in patients with early Parkinson’s Disease. Movement Disorders, 27(1), 98–105.PubMedCrossRef
go back to reference Schmahmann, J. D., & Sherman, J. C. (1998). The cerebellar cognitive affective syndrome. Brain, 121(4), 561–579.PubMedCrossRef Schmahmann, J. D., & Sherman, J. C. (1998). The cerebellar cognitive affective syndrome. Brain, 121(4), 561–579.PubMedCrossRef
go back to reference Schneider, A., Ballinger, E., Chavez, A., Tassone, F., Hagerman, R. J., & Hessl, D. (2012). Prepulse inhibition in patients with fragile X-associated tremor ataxia syndrome. Neurobiology of Aging, 33(6), 1045–1053.PubMedCentralPubMedCrossRef Schneider, A., Ballinger, E., Chavez, A., Tassone, F., Hagerman, R. J., & Hessl, D. (2012). Prepulse inhibition in patients with fragile X-associated tremor ataxia syndrome. Neurobiology of Aging, 33(6), 1045–1053.PubMedCentralPubMedCrossRef
go back to reference Seritan, A. L., Nguyen, D. V., Farias, S. T., Hinton, L., Grigsby, J., Bourgeois, J. A., et al. (2008). Dementia in fragile X-associated tremor/ataxia syndrome (FXTAS): comparison with Alzheimer’s disease. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 147B(7), 1138–1144.CrossRef Seritan, A. L., Nguyen, D. V., Farias, S. T., Hinton, L., Grigsby, J., Bourgeois, J. A., et al. (2008). Dementia in fragile X-associated tremor/ataxia syndrome (FXTAS): comparison with Alzheimer’s disease. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 147B(7), 1138–1144.CrossRef
go back to reference Sevin, M., Kutalik, Z., Bergman, S., Vercelletto, M., Renou, P., Lamy, E., et al. (2009). Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation. Journal of Medical Genetics, 46(12), 818–824.PubMedCrossRef Sevin, M., Kutalik, Z., Bergman, S., Vercelletto, M., Renou, P., Lamy, E., et al. (2009). Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation. Journal of Medical Genetics, 46(12), 818–824.PubMedCrossRef
go back to reference Sharman, M., Valabregue, R., Perlbarg, V., Marrakchi-Kacem, L., Vidailhet, M., Benali, H., et al. (2013). Parkinson’s Disease patients show reduced cortical-subcortical sensorimotor connectivity. Movement Disorders, 28(4), 447–454.PubMedCrossRef Sharman, M., Valabregue, R., Perlbarg, V., Marrakchi-Kacem, L., Vidailhet, M., Benali, H., et al. (2013). Parkinson’s Disease patients show reduced cortical-subcortical sensorimotor connectivity. Movement Disorders, 28(4), 447–454.PubMedCrossRef
go back to reference Shiba, M., Bower, J. H., Maraganore, D. M., McDonnell, S. K., Peterson, B. J., Ahlskog, J. E., et al. (2000). Anxiety disorders and depressive disorders preceding Parkinson’s Disease: a case–control study. Movement Disorders, 15(4), 669–677.PubMedCrossRef Shiba, M., Bower, J. H., Maraganore, D. M., McDonnell, S. K., Peterson, B. J., Ahlskog, J. E., et al. (2000). Anxiety disorders and depressive disorders preceding Parkinson’s Disease: a case–control study. Movement Disorders, 15(4), 669–677.PubMedCrossRef
go back to reference Sobesky, W. E., Hull, C. E., & Hagerman, R. J. (1994). Symptoms of schizotypal personality disorder in fragile X women. Journal of the American Academy of Child & Adolescent Psychiatry, 33(2), 247–255.CrossRef Sobesky, W. E., Hull, C. E., & Hagerman, R. J. (1994). Symptoms of schizotypal personality disorder in fragile X women. Journal of the American Academy of Child & Adolescent Psychiatry, 33(2), 247–255.CrossRef
go back to reference Storey, E., & Billimoria, P. (2005). Increased T2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome. Journal of Clinical Neuroscience, 12(1), 42–43.PubMedCrossRef Storey, E., & Billimoria, P. (2005). Increased T2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome. Journal of Clinical Neuroscience, 12(1), 42–43.PubMedCrossRef
go back to reference Strick, P. L., Dum, R. P., & Fiez, J. A. (2009). Cerebellum and nonmotor function. Annual Review of Neuroscience, 32, 413–434.PubMedCrossRef Strick, P. L., Dum, R. P., & Fiez, J. A. (2009). Cerebellum and nonmotor function. Annual Review of Neuroscience, 32, 413–434.PubMedCrossRef
go back to reference Tassone, F., Iong, K. P., Tong, T., Lo, J., Gane, L. W., Berry-Kravis, E., et al. (2012a). FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States. Genome Medicine, 4(12), 100.PubMedCentralPubMedCrossRef Tassone, F., Iong, K. P., Tong, T., Lo, J., Gane, L. W., Berry-Kravis, E., et al. (2012a). FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States. Genome Medicine, 4(12), 100.PubMedCentralPubMedCrossRef
go back to reference Tassone, F., Greco, C. M., Hunsaker, M. R., Seritan, A. L., Berman, R. F., Gane, L. W., et al. (2012b). Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS. Genes, Brain and Behavior, 11(5), 577–585.CrossRef Tassone, F., Greco, C. M., Hunsaker, M. R., Seritan, A. L., Berman, R. F., Gane, L. W., et al. (2012b). Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS. Genes, Brain and Behavior, 11(5), 577–585.CrossRef
go back to reference Tovar-Moll, F., Evangelou, I. E., Chiu, A. W., Richert, N. D., Ostuni, J. L., Ohayon, J. M., et al. (2009). Thalamic involvement and its impact on clinical disability in patients with multiple sclerosis: A diffusion tensor imaging study at 3T. American Journal of Neuroradiology, 30(7), 1380–1386.PubMedCrossRef Tovar-Moll, F., Evangelou, I. E., Chiu, A. W., Richert, N. D., Ostuni, J. L., Ohayon, J. M., et al. (2009). Thalamic involvement and its impact on clinical disability in patients with multiple sclerosis: A diffusion tensor imaging study at 3T. American Journal of Neuroradiology, 30(7), 1380–1386.PubMedCrossRef
go back to reference Wang, J., Hessl, D., Schneider, A., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2013a). Fragile X associated tremor/ataxia syndrome: Influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles. JAMA Neurology, 70(8), 1022–1029.PubMedCentralPubMedCrossRef Wang, J., Hessl, D., Schneider, A., Tassone, F., Hagerman, R. J., & Rivera, S. M. (2013a). Fragile X associated tremor/ataxia syndrome: Influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles. JAMA Neurology, 70(8), 1022–1029.PubMedCentralPubMedCrossRef
go back to reference Wang, J. Y., Hagerman, R. J., & Rivera, S. (2013b). A multimodal imaging analysis of subcortical gray matter in fragile X premutation carriers. Movement Disorders, 28(9), 1278–1284.PubMedCentralPubMedCrossRef Wang, J. Y., Hagerman, R. J., & Rivera, S. (2013b). A multimodal imaging analysis of subcortical gray matter in fragile X premutation carriers. Movement Disorders, 28(9), 1278–1284.PubMedCentralPubMedCrossRef
go back to reference Wechsler, D. (1997). WAIS-III administration and scoring manual. San Antonio: The Psychological Corporation. Wechsler, D. (1997). WAIS-III administration and scoring manual. San Antonio: The Psychological Corporation.
go back to reference Yang, J. C., Chan, S.-H., Khan, S., Schneider, A., Nanakul, R., Teichholtz, S., et al. (2013a). Neural substrates of executive dysfunction in fragile X-associated tremor/ataxia syndrome (FXTAS): a brain potential study. Cerebral Cortex, 23(11), 2657–2666.PubMedCentralPubMedCrossRef Yang, J. C., Chan, S.-H., Khan, S., Schneider, A., Nanakul, R., Teichholtz, S., et al. (2013a). Neural substrates of executive dysfunction in fragile X-associated tremor/ataxia syndrome (FXTAS): a brain potential study. Cerebral Cortex, 23(11), 2657–2666.PubMedCentralPubMedCrossRef
go back to reference Yang, J. C., Simon, C., Niu, Y.-Q., Bogost, M., Schneider, A., Tassone, F., et al. (2013b). Phenotypes of hypofrontality in older female fragile x premutation carriers. Annals of Neurology, 74(2), 275–283. Yang, J. C., Simon, C., Niu, Y.-Q., Bogost, M., Schneider, A., Tassone, F., et al. (2013b). Phenotypes of hypofrontality in older female fragile x premutation carriers. Annals of Neurology, 74(2), 275–283.
go back to reference Zgaljardic, D. J., Borod, J. C., Foldi, N. S., Mattis, P. J., Gordon, M. F., Feigin, A., et al. (2006). An examination of executive dysfunction associated with frontostriatal circuitry in Parkinson’s Disease. Journal of Clinical and Experimental Neuropsychology, 28(7), 1127–1144.PubMedCrossRef Zgaljardic, D. J., Borod, J. C., Foldi, N. S., Mattis, P. J., Gordon, M. F., Feigin, A., et al. (2006). An examination of executive dysfunction associated with frontostriatal circuitry in Parkinson’s Disease. Journal of Clinical and Experimental Neuropsychology, 28(7), 1127–1144.PubMedCrossRef
go back to reference Zhang, L., Coffey, S., Lua, L. L., Greco, C. M., Schafer, J. A., Brunberg, J., et al. (2009). FMR1 premutation in females diagnosed with multiple sclerosis. Journal of Neurology, Neurosurgery & Psychiatry, 80(7), 812–814.CrossRef Zhang, L., Coffey, S., Lua, L. L., Greco, C. M., Schafer, J. A., Brunberg, J., et al. (2009). FMR1 premutation in females diagnosed with multiple sclerosis. Journal of Neurology, Neurosurgery & Psychiatry, 80(7), 812–814.CrossRef
go back to reference Zhang, X., Zhuang, X., Gan, S., Wu, Z., Chen, W., Hu, Y., et al. (2012). Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China. Neuroscience Letters, 514(1), 16–21.PubMedCrossRef Zhang, X., Zhuang, X., Gan, S., Wu, Z., Chen, W., Hu, Y., et al. (2012). Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China. Neuroscience Letters, 514(1), 16–21.PubMedCrossRef
go back to reference Zuhlke, C., Budnik, A., Gehlken, U., Dalski, A., Purmann, S., Naumann, M., et al. (2004). FMR1 premutation as a rare cause of late onset ataxia. Journal of Neurology, 251(11), 1418–1419.PubMedCrossRef Zuhlke, C., Budnik, A., Gehlken, U., Dalski, A., Purmann, S., Naumann, M., et al. (2004). FMR1 premutation as a rare cause of late onset ataxia. Journal of Neurology, 251(11), 1418–1419.PubMedCrossRef
Metadata
Title
Understanding the Neuropsychiatric Phenotype of Fragile X-Associated Tremor Ataxia Syndrome: a Systematic Review
Authors
R. C. Birch
K. M. Cornish
D. R. Hocking
J. N. Trollor
Publication date
01-12-2014
Publisher
Springer US
Published in
Neuropsychology Review / Issue 4/2014
Print ISSN: 1040-7308
Electronic ISSN: 1573-6660
DOI
https://doi.org/10.1007/s11065-014-9262-9

Other articles of this Issue 4/2014

Neuropsychology Review 4/2014 Go to the issue