Skip to main content
Top
Published in: Italian Journal of Pediatrics 1/2010

Open Access 01-12-2010 | Review

Epilepsy in patients with Angelman syndrome

Authors: Agata Fiumara, Annarita Pittalà, Mariadonatella Cocuzza, Giovanni Sorge

Published in: Italian Journal of Pediatrics | Issue 1/2010

Login to get access

Abstract

Angelman syndrome (AS) is a neuro-behavioural, genetically determined condition, characterized by ataxic jerky movements, happy sociable disposition and unprovoked bouts of laughter in association with seizures, learning disabilities and language impairment. Most of the cases are hardly diagnosed during infancy as jerky movements, the cardinal sign, appear later in childhood.
AS is caused by a variety of genetic mechanisms involving the 15q 11-13 chromosome. About 70% of cases are due to a "de novo" interstitial deletion in the long arm region, arising on the maternally inherited chromosome. The diagnosis is confirmed by methylation test or by mutation analysis of UBE3A gene. The deletion phenotype is generally linked to a more severe clinical picture in that 95% of patients manifest more severe seizures, severe mental and motor retardation, dysmorphic features and microcephaly.
The pathogenesis of epilepsy in AS is still not fully understood. The presence in the commonly deleted region of a cluster of genes coding for 3 subunits of the GABAa receptor complex has lead to the hypothesis that GABA neurotransmission is involved.
Epilepsy, often severe and hard to control, is present in 85% of patients within the first three years of life, although less than 25% develop seizures during the first year. It was observed that febrile seizures often precede the diagnosis. Most frequent types are atypical absences, generalized tonic-clonic, atonic or myoclonic seizures, with multiple seizure types occurring in 50% of deleted patients. There is still some doubt about the association with West syndrome.
The EEG abnormalities are not themselves pathognomonic of AS and both background activity and epileptic discharges vary even in the same patient with time. Nevertheless, the existence of some suggestive patterns should facilitate the early diagnosis allowing the correct genetic counselling for the family. Some drugs seems to act better than others, Valproate, ethosuximide and clonazepam giving the best results.
Appendix
Available only for authorised users
Literature
1.
go back to reference Angelman H: "Puppet children" a report of three cases. Dev Med Child Neurol. 1965, 7: 681-688.CrossRef Angelman H: "Puppet children" a report of three cases. Dev Med Child Neurol. 1965, 7: 681-688.CrossRef
2.
go back to reference Robb SA, Pohl KRE, Baraitser M, Wilson J, Brett EM: The "happy puppet" syndrome of Angelman: review of the clinical features. Arch Dis Child. 1989, 64: 83-86. 10.1136/adc.64.1.83.PubMedCentralPubMedCrossRef Robb SA, Pohl KRE, Baraitser M, Wilson J, Brett EM: The "happy puppet" syndrome of Angelman: review of the clinical features. Arch Dis Child. 1989, 64: 83-86. 10.1136/adc.64.1.83.PubMedCentralPubMedCrossRef
3.
go back to reference Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Pembrey ME, Malcom S, Nicholls RD: Differences in methylation pattern within the D15S9 region of chromosome 15q11-q13 in first cousins with Angelman and Prader Willi syndromes. Am J Med Genet. 1993, 47: 683-686. 10.1002/ajmg.1320470519.PubMedCrossRef Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Pembrey ME, Malcom S, Nicholls RD: Differences in methylation pattern within the D15S9 region of chromosome 15q11-q13 in first cousins with Angelman and Prader Willi syndromes. Am J Med Genet. 1993, 47: 683-686. 10.1002/ajmg.1320470519.PubMedCrossRef
4.
go back to reference Williams CA: Angelman Syndrome. Management of Genetic Syndromes. Edited by: Cassidy SB, Allanson JE. 2005, Wiley-Liss Inch, 53-62. 2 Williams CA: Angelman Syndrome. Management of Genetic Syndromes. Edited by: Cassidy SB, Allanson JE. 2005, Wiley-Liss Inch, 53-62. 2
5.
go back to reference Knoll JHM, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA: Angelman and Prader Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am J Med Genet. 1989, 32: 285-290. 10.1002/ajmg.1320320235.PubMedCrossRef Knoll JHM, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA: Angelman and Prader Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am J Med Genet. 1989, 32: 285-290. 10.1002/ajmg.1320320235.PubMedCrossRef
6.
go back to reference Malcom S, Clayton-Smith J, Nichols M, Robb S, Webb T, Armour JAL, Jeffreys AJ, Pembrey ME: Uniparental paternal disomy in Angelman's syndrome. Lancet. 1991, 337: 694-697. 10.1016/0140-6736(91)90278-W.CrossRef Malcom S, Clayton-Smith J, Nichols M, Robb S, Webb T, Armour JAL, Jeffreys AJ, Pembrey ME: Uniparental paternal disomy in Angelman's syndrome. Lancet. 1991, 337: 694-697. 10.1016/0140-6736(91)90278-W.CrossRef
7.
go back to reference Buiting K, Saitoh S, Gross S, Schwartz S, Nicholls RD, Horsthemke B: Inherited microdeletions in Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet. 1995, 9: 395-400. 10.1038/ng0495-395.PubMedCrossRef Buiting K, Saitoh S, Gross S, Schwartz S, Nicholls RD, Horsthemke B: Inherited microdeletions in Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet. 1995, 9: 395-400. 10.1038/ng0495-395.PubMedCrossRef
8.
go back to reference Kishino T, Lalande M, Wagstaff J: UBE3A/E6-AP mutations cause Angelmann Syndrome. Nat Genet. 1997, 15: 70-73. 10.1038/ng0197-70.PubMedCrossRef Kishino T, Lalande M, Wagstaff J: UBE3A/E6-AP mutations cause Angelmann Syndrome. Nat Genet. 1997, 15: 70-73. 10.1038/ng0197-70.PubMedCrossRef
9.
go back to reference Matsuura T, Sutcliffe JS, Fang P, Galjaard RJ, Jiang YH, Benton CS, Rommens JM, Beaudet AL: De novo truncating mutations in E6-AP ubiquitin-protein ligase (UBE3A) in Angelman syndrome. Nature Genet. 1997, 15: 74-77. 10.1038/ng0197-74.PubMedCrossRef Matsuura T, Sutcliffe JS, Fang P, Galjaard RJ, Jiang YH, Benton CS, Rommens JM, Beaudet AL: De novo truncating mutations in E6-AP ubiquitin-protein ligase (UBE3A) in Angelman syndrome. Nature Genet. 1997, 15: 74-77. 10.1038/ng0197-74.PubMedCrossRef
10.
go back to reference Rougelle C, Glatt H, Lalande M: The Angelman syndrome candidate gene UBE3A/E6AP is imprinted in brain. Nat Genet. 1997, 17: 14-15. 10.1038/ng0997-14.CrossRef Rougelle C, Glatt H, Lalande M: The Angelman syndrome candidate gene UBE3A/E6AP is imprinted in brain. Nat Genet. 1997, 17: 14-15. 10.1038/ng0997-14.CrossRef
11.
go back to reference Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, Hutson A, Nicholls RD, Zori RT, Williams CA, Driscoll DJ: Distinct phenotypes distinguish the molecular classes of Angelman syndrome. J Med Genet. 2001, 38: 834-835. 10.1136/jmg.38.12.834.PubMedCentralPubMedCrossRef Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, Hutson A, Nicholls RD, Zori RT, Williams CA, Driscoll DJ: Distinct phenotypes distinguish the molecular classes of Angelman syndrome. J Med Genet. 2001, 38: 834-835. 10.1136/jmg.38.12.834.PubMedCentralPubMedCrossRef
12.
go back to reference Minassian BA, DeLorey TM, Olsen RW, Philippart M, Bronstein Y, Zhang Q, Guerrini R, Van Ness P, Livet MO, Delgado-Escueta AV: Angelman Syndrome: correlations between epilepsy phenotypes and genotypes. Ann Neurol. 1998, 43: 485-493. 10.1002/ana.410430412.PubMedCrossRef Minassian BA, DeLorey TM, Olsen RW, Philippart M, Bronstein Y, Zhang Q, Guerrini R, Van Ness P, Livet MO, Delgado-Escueta AV: Angelman Syndrome: correlations between epilepsy phenotypes and genotypes. Ann Neurol. 1998, 43: 485-493. 10.1002/ana.410430412.PubMedCrossRef
13.
go back to reference Nicholls RD, Saitoh S, Horsthemke B: Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 1998, 14: 194-200. 10.1016/S0168-9525(98)01432-2.PubMedCrossRef Nicholls RD, Saitoh S, Horsthemke B: Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 1998, 14: 194-200. 10.1016/S0168-9525(98)01432-2.PubMedCrossRef
14.
go back to reference Dan B, Boyd SG: Angelman syndrome reviewed from a neurophysiological perspective. The UBE3A-GABRB3 hypothesis. Neuropediatrics. 2003, 34: 169-176. 10.1055/s-2003-42213.PubMedCrossRef Dan B, Boyd SG: Angelman syndrome reviewed from a neurophysiological perspective. The UBE3A-GABRB3 hypothesis. Neuropediatrics. 2003, 34: 169-176. 10.1055/s-2003-42213.PubMedCrossRef
15.
go back to reference Dan B: Angelman syndrome: Current understanding and research prospects. Epilepsia. 2009, 50 (11): 2331-2339. 10.1111/j.1528-1167.2009.02311.x.PubMedCrossRef Dan B: Angelman syndrome: Current understanding and research prospects. Epilepsia. 2009, 50 (11): 2331-2339. 10.1111/j.1528-1167.2009.02311.x.PubMedCrossRef
16.
go back to reference Samaco RC, Hogart A, LaSalle JM: Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum Mol Genet. 2005, 14 (4): 483-92. 10.1093/hmg/ddi045.PubMedCentralPubMedCrossRef Samaco RC, Hogart A, LaSalle JM: Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum Mol Genet. 2005, 14 (4): 483-92. 10.1093/hmg/ddi045.PubMedCentralPubMedCrossRef
17.
go back to reference Clayton-Smith J: Clinical research on Angelman syndrome in the United Kingdom: observation on 82 affected individuals. Am J Med Genet. 1993, 46: 12-15. 10.1002/ajmg.1320460105.PubMedCrossRef Clayton-Smith J: Clinical research on Angelman syndrome in the United Kingdom: observation on 82 affected individuals. Am J Med Genet. 1993, 46: 12-15. 10.1002/ajmg.1320460105.PubMedCrossRef
18.
go back to reference Saitoh S, Harada N, Jinno Y, Hashimoto K, Imaizumi K, Kuroki Y, Fukushima Y, Sugimoto T, Renedo M, Wagstaff J, Lalande M, Mutirangura A, Kuwano A, Ledbetter DH, Nikawa N: Molecular and clinical study of 61 Angelman syndrome patients. Am J Med Genet. 1994, 52: 158-163. 10.1002/ajmg.1320520207.PubMedCrossRef Saitoh S, Harada N, Jinno Y, Hashimoto K, Imaizumi K, Kuroki Y, Fukushima Y, Sugimoto T, Renedo M, Wagstaff J, Lalande M, Mutirangura A, Kuwano A, Ledbetter DH, Nikawa N: Molecular and clinical study of 61 Angelman syndrome patients. Am J Med Genet. 1994, 52: 158-163. 10.1002/ajmg.1320520207.PubMedCrossRef
19.
go back to reference Matsumoto A, Kumagai T, Miura K, Myazaki S, Hayakawa C, Yamanaka T: Epilepsy in Angelman syndrome associated with chromosome 15q deletion. Epilepsia. 1992, 33 (6): 1083-1090. 10.1111/j.1528-1157.1992.tb01763.x.PubMedCrossRef Matsumoto A, Kumagai T, Miura K, Myazaki S, Hayakawa C, Yamanaka T: Epilepsy in Angelman syndrome associated with chromosome 15q deletion. Epilepsia. 1992, 33 (6): 1083-1090. 10.1111/j.1528-1157.1992.tb01763.x.PubMedCrossRef
20.
go back to reference Viani F, Romeo A, Viri M, Mastrangelo M, Lalatta F, Selicorni A, Gobbi G, Lanzi G, Bettio D, Briscioli V: Seizures and EEG pattern in Angelman syndrome. J Chid Neurol. 1995, 10 (6): 467-471. 10.1177/088307389501000609.CrossRef Viani F, Romeo A, Viri M, Mastrangelo M, Lalatta F, Selicorni A, Gobbi G, Lanzi G, Bettio D, Briscioli V: Seizures and EEG pattern in Angelman syndrome. J Chid Neurol. 1995, 10 (6): 467-471. 10.1177/088307389501000609.CrossRef
21.
go back to reference Guerrini R, Carrozzo R, Rinaldi R, Bonanni P: Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms. Paediatr Drugs. 2003, 5 (10): 647-661. 10.2165/00148581-200305100-00001.PubMedCrossRef Guerrini R, Carrozzo R, Rinaldi R, Bonanni P: Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms. Paediatr Drugs. 2003, 5 (10): 647-661. 10.2165/00148581-200305100-00001.PubMedCrossRef
22.
go back to reference Valente KD, Koiffmann CP, Fridman C, Varella M, Kok F, Andrade JQ, Grossmann RM, Marques-Dias MJ: Epilepsy in patients with Angelman syndrome caused by deletion of the chromosome 15q11-q13. Arch Neurol. 2006, 63: 122-128. 10.1001/archneur.63.1.122.PubMedCrossRef Valente KD, Koiffmann CP, Fridman C, Varella M, Kok F, Andrade JQ, Grossmann RM, Marques-Dias MJ: Epilepsy in patients with Angelman syndrome caused by deletion of the chromosome 15q11-q13. Arch Neurol. 2006, 63: 122-128. 10.1001/archneur.63.1.122.PubMedCrossRef
23.
go back to reference Buoni S, Grosso S, Pucci L, Fois A: Diagnosis of Angelman syndrome: clinical and EEG criteria. Brain Dev. 1999, 21: 296-302. 10.1016/S0387-7604(99)00007-8.PubMedCrossRef Buoni S, Grosso S, Pucci L, Fois A: Diagnosis of Angelman syndrome: clinical and EEG criteria. Brain Dev. 1999, 21: 296-302. 10.1016/S0387-7604(99)00007-8.PubMedCrossRef
24.
go back to reference Galvan-Manso M, Campistol J, Conill J, Sanmartì FX: Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome. Epileptic Disord. 2005, 7 (1): 19-25.PubMed Galvan-Manso M, Campistol J, Conill J, Sanmartì FX: Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome. Epileptic Disord. 2005, 7 (1): 19-25.PubMed
25.
go back to reference Pelc K, Boyd SG, Cheron G, Dan B: Epilepsy in Angelman syndrome. Seizure. 2008, 17: 211-217. 10.1016/j.seizure.2007.08.004.PubMedCrossRef Pelc K, Boyd SG, Cheron G, Dan B: Epilepsy in Angelman syndrome. Seizure. 2008, 17: 211-217. 10.1016/j.seizure.2007.08.004.PubMedCrossRef
26.
go back to reference Elia M: Myoclonic status in nonprogressive envephalopathies: an update. Epilepsia. 2009, 50 (suppl.5): 41-44. 10.1111/j.1528-1167.2009.02119.x.PubMedCrossRef Elia M: Myoclonic status in nonprogressive envephalopathies: an update. Epilepsia. 2009, 50 (suppl.5): 41-44. 10.1111/j.1528-1167.2009.02119.x.PubMedCrossRef
27.
go back to reference Valente KD: Another Rett patient with a Typical Angelman EEG. Epilepsia. 2003, 44 (6): 873-874. 10.1046/j.1528-1157.2003.04803_3.x.PubMedCrossRef Valente KD: Another Rett patient with a Typical Angelman EEG. Epilepsia. 2003, 44 (6): 873-874. 10.1046/j.1528-1157.2003.04803_3.x.PubMedCrossRef
28.
go back to reference Boyd SG, Harden A, Patton MA: The EEG in early diagnosis of Angelman syndrome. Eur J Pediatr. 1988, 147: 508-513. 10.1007/BF00441976.PubMedCrossRef Boyd SG, Harden A, Patton MA: The EEG in early diagnosis of Angelman syndrome. Eur J Pediatr. 1988, 147: 508-513. 10.1007/BF00441976.PubMedCrossRef
29.
go back to reference Laan LAEM, Vein AA: Angelman syndrome: is there a characteristic EEG?. Brain Develop. 2005, 27: 80-87. 10.1016/j.braindev.2003.09.013.CrossRef Laan LAEM, Vein AA: Angelman syndrome: is there a characteristic EEG?. Brain Develop. 2005, 27: 80-87. 10.1016/j.braindev.2003.09.013.CrossRef
30.
go back to reference Valente KDF, Andrade JQ, Grossmann RM, Kok F, Fridman C, Koiffman CP, Marques-Dias MJ: Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretations. Epilepsia. 2003, 44 (8): 1051-1063. 10.1046/j.1528-1157.2003.66502.x.PubMedCrossRef Valente KDF, Andrade JQ, Grossmann RM, Kok F, Fridman C, Koiffman CP, Marques-Dias MJ: Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretations. Epilepsia. 2003, 44 (8): 1051-1063. 10.1046/j.1528-1157.2003.66502.x.PubMedCrossRef
31.
go back to reference Ostergaard JR, Balslev T: Efficacy of different antiepileptic drugs in children with Angelman syndrome associated with 15q11-13 deletion: the Danish experience. Dev Med Child Neurol. 2001, 43: 718-719. 10.1017/S0012162201001293.PubMedCrossRef Ostergaard JR, Balslev T: Efficacy of different antiepileptic drugs in children with Angelman syndrome associated with 15q11-13 deletion: the Danish experience. Dev Med Child Neurol. 2001, 43: 718-719. 10.1017/S0012162201001293.PubMedCrossRef
32.
go back to reference Franz DN, Glauser TA, Tudor C, Williams S: Topiramate therapy of epilepsy associated with Angelman syndrome. Neurology. 2000, 54: 1185-1188.PubMedCrossRef Franz DN, Glauser TA, Tudor C, Williams S: Topiramate therapy of epilepsy associated with Angelman syndrome. Neurology. 2000, 54: 1185-1188.PubMedCrossRef
33.
go back to reference Sugiura C, Ogura K, Ueno M, Toyoshima M, Oka A: High dose ethosuximide for epilepsy in Angelman syndrome: implication of GABA(A) receptor subunit. Neurology. 2001, 57: 1518-1519.PubMedCrossRef Sugiura C, Ogura K, Ueno M, Toyoshima M, Oka A: High dose ethosuximide for epilepsy in Angelman syndrome: implication of GABA(A) receptor subunit. Neurology. 2001, 57: 1518-1519.PubMedCrossRef
34.
go back to reference Dion MH, Novotny EJ, Carmant L, Cossette P, Nguyen DK: Lamotrigine therapy of epilepsy with Angelman syndrome. Epilepsia. 2007, 48 (3): 593-596. 10.1111/j.1528-1167.2006.00969.x.PubMedCrossRef Dion MH, Novotny EJ, Carmant L, Cossette P, Nguyen DK: Lamotrigine therapy of epilepsy with Angelman syndrome. Epilepsia. 2007, 48 (3): 593-596. 10.1111/j.1528-1167.2006.00969.x.PubMedCrossRef
35.
go back to reference Forrest KML, Young H, Dale RC, Gill DS: Benefit of corticosteroid therapy in Angelman Syndrome. J Child Neurol. 2009, 24 (8): 952-958. 10.1177/0883073808331344.PubMedCrossRef Forrest KML, Young H, Dale RC, Gill DS: Benefit of corticosteroid therapy in Angelman Syndrome. J Child Neurol. 2009, 24 (8): 952-958. 10.1177/0883073808331344.PubMedCrossRef
36.
go back to reference Pitt D, Hopkins I: A syndrome of mental retardation, wide mouth and intermittent overbreathing. Austr Ped J. 1978, 14: 182-184. Pitt D, Hopkins I: A syndrome of mental retardation, wide mouth and intermittent overbreathing. Austr Ped J. 1978, 14: 182-184.
37.
go back to reference Rosenfeld JA, Leppig K, Ballif BC, Thiese H, Erdie-Lalena C, Bawle E, Sastry S, Spence JE, Bandholz A, Surti U, Zonana J, Keller K, Meschino W, Bejjani BA, Torchia BS, Shaffer LG: Genotype-phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations. Genet Med. 2009, 11 (11): 797-805. 10.1097/GIM.0b013e3181bd38a9.PubMedCrossRef Rosenfeld JA, Leppig K, Ballif BC, Thiese H, Erdie-Lalena C, Bawle E, Sastry S, Spence JE, Bandholz A, Surti U, Zonana J, Keller K, Meschino W, Bejjani BA, Torchia BS, Shaffer LG: Genotype-phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations. Genet Med. 2009, 11 (11): 797-805. 10.1097/GIM.0b013e3181bd38a9.PubMedCrossRef
38.
go back to reference Laan LAEM, Renier WO, Arts WFM, Buntinx IM, vd Burgt IJAM, Stroink H, Beuten J, Zwinderman KH: Evolution of epilepsy and EEG findings in Angelman syndrome. Epilepsia. 1997, 38: 195-199. 10.1111/j.1528-1157.1997.tb01097.x.PubMedCrossRef Laan LAEM, Renier WO, Arts WFM, Buntinx IM, vd Burgt IJAM, Stroink H, Beuten J, Zwinderman KH: Evolution of epilepsy and EEG findings in Angelman syndrome. Epilepsia. 1997, 38: 195-199. 10.1111/j.1528-1157.1997.tb01097.x.PubMedCrossRef
Metadata
Title
Epilepsy in patients with Angelman syndrome
Authors
Agata Fiumara
Annarita Pittalà
Mariadonatella Cocuzza
Giovanni Sorge
Publication date
01-12-2010
Publisher
BioMed Central
Published in
Italian Journal of Pediatrics / Issue 1/2010
Electronic ISSN: 1824-7288
DOI
https://doi.org/10.1186/1824-7288-36-31

Other articles of this Issue 1/2010

Italian Journal of Pediatrics 1/2010 Go to the issue