Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11886
Title: Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.
Authors: Mullen, Saul A;Carvill, Gemma L;Bellows, Susannah;Bayly, Marta A;Trucks, Holger;Lal, Dennis;Sander, Thoman;Berkovic, Samuel F;Dibbens, Leanne M;Scheffer, Ingrid E;Mefford, Heather C
Affiliation: From the Florey Institute of Neuroscience and Mental Health (S.A.M., I.E.S.), Epilepsy Research Centre, Department of Medicine, Austin and Northern Health (S.B., S.F.B., I.E.S.), and Department of Paediatrics, Royal Children's Hospital (I.E.S.), University of Melbourne, Australia
Department of Pediatrics (G.L.C., H.C.M.), Division of Genetic Medicine, University of Washington, Seattle; and Epilepsy Research Program, School of Pharmacy and Medical Sciences (M.A.B., L.M.D.), and Sansom Institute for Health Research (M.A.B., L.M.D.), University of South Australia, Adelaide.
Issue Date: 25-Sep-2013
Citation: Neurology 2013; 81(17): 1507-14
Abstract: We examined whether copy number variants (CNVs) were more common in those with a combination of intellectual disability (ID) and genetic generalized epilepsy (GGE) than in those with either phenotype alone via a case-control study.CNVs contribute to the genetics of multiple neurodevelopmental disorders with complex inheritance, including GGE and ID. Three hundred fifty-nine probands with GGE and 60 probands with ID-GGE were screened for GGE-associated recurrent microdeletions at 15q13.3, 15q11.2, and 16p13.11 via quantitative PCR or loss of heterozygosity. Deletions were confirmed by comparative genomic hybridization (CGH). ID-GGE probands also had genome-wide CGH.ID-GGE probands showed a significantly higher rate of CNVs compared with probands with GGE alone, with 17 of 60 (28%) ID-GGE probands having one or more potentially causative CNVs. The patients with ID-GGE had a 3-fold-higher rate of the 3 GGE-associated recurrent microdeletions than probands with GGE alone (10% vs 3%, p = 0.02). They also showed a high rate (13/60, 22%) of rare CNVs identified using genome-wide CGH.This study shows that CNVs are common in those with ID-GGE with recurrent deletions at 15q13.3, 15q11.2, and 16p13.11, particularly enriched compared with individuals with GGE or ID alone. Recurrent CNVs are likely to act as risk factors for multiple phenotypes not just at the population level, but also in any given individual. Testing for CNVs in ID-GGE will have a high diagnostic yield in a clinical setting and will inform genetic counseling.
Internal ID Number: 24068782
URI: http://ahro.austin.org.au/austinjspui/handle/1/11886
DOI: 10.1212/WNL.0b013e3182a95829
URL: http://www.ncbi.nlm.nih.gov/pubmed/24068782
Type: Journal Article
Subjects: Adolescent
Adult
Aged
Case-Control Studies
Child
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders.genetics
Chromosomes, Human, Pair 15.genetics
Chromosomes, Human, Pair 16.genetics
Cohort Studies
Comorbidity
DNA Copy Number Variations.genetics
Epilepsy, Generalized.epidemiology.genetics
Female
Genetic Testing
Humans
Intellectual Disability.epidemiology.genetics
Male
Middle Aged
Phenotype
Rubinstein-Taybi Syndrome.genetics
Seizures.genetics
Young Adult
Appears in Collections:Journal articles

Files in This Item:
There are no files associated with this item.


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.