Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/9728
Title: Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
Authors: Marini, Carla;Scheffer, Ingrid E;Crossland, Kathryn M;Grinton, Bronwyn E;Phillips, Fiona L;McMahon, Jacinta M;Turner, Samantha J;Dean, Joanne T;Kivity, Sara;Mazarib, Aziz;Neufeld, Miriam Y;Korczyn, Amos D;Harkin, Louise A;Dibbens, Leanne M;Wallace, Robyn H;Mulley, John C;Berkovic, Samuel F
Affiliation: Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne, Austin Health, Victoria, Australia.
Issue Date: 1-May-2004
Citation: Epilepsia; 45(5): 467-78
Abstract: In families with idiopathic generalized epilepsy (IGE), multiple IGE subsyndromes may occur. We performed a genetic study of IGE families to clarify the genetic relation of the IGE subsyndromes and to improve understanding of the mode(s) of inheritance.Clinical and genealogic data were obtained on probands with IGE and family members with a history of seizures. Families were grouped according to the probands' IGE subsyndrome: childhood absence epilepsy (CAE), juvenile absence epilepsy (JAE), juvenile myoclonic epilepsy (JME), and IGE with tonic-clonic seizures only (IGE-TCS). The subsyndromes in the relatives were analyzed. Mutations in genes encoding alpha1 and gamma 2 gamma-aminobutyric acid (GABA)-receptor subunits, alpha1 and beta1 sodium channel subunits, and the chloride channel CLC-2 were sought.Fifty-five families were studied. 122 (13%) of 937 first- and second-degree relatives had seizures. Phenotypic concordance within families of CAE and JME probands was 28 and 27%, respectively. JAE and IGE-TCS families had a much lower concordance (10 and 13%), and in the JAE group, 31% of relatives had CAE. JME was rare among affected relatives of CAE and JAE probands and vice versa. Mothers were more frequently affected than fathers. No GABA-receptor or sodium or chloride channel gene mutations were identified.The clinical genetic analysis of this set of families suggests that CAE and JAE share a close genetic relation, whereas JME is a more distinct entity. Febrile seizures and epilepsy with unclassified tonic-clonic seizures were frequent in affected relatives of all IGE individuals, perhaps representing a nonspecific susceptibility to seizures. A maternal effect also was seen. Our findings are consistent with an oligogenic model of inheritance.
Internal ID Number: 15101828
URI: http://ahro.austin.org.au/austinjspui/handle/1/9728
DOI: 10.1111/j.0013-9580.2004.46803.x
URL: http://www.ncbi.nlm.nih.gov/pubmed/15101828
Type: Journal Article
Subjects: Adolescent
Adult
Child
Chloride Channels.genetics
Epilepsy, Absence.genetics
Epilepsy, Generalized.genetics
Family
Female
Gene Frequency.genetics
Genetic Heterogeneity
Genetic Linkage
Genetic Predisposition to Disease
Genotype
Humans
Male
Models, Genetic
Mutation
Myoclonic Epilepsy, Juvenile.genetics
Pedigree
Phenotype
Receptors, GABA.genetics
Sodium Channels.genetics
Appears in Collections:Journal articles

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