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Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.
- Source :
-
Epilepsy research [Epilepsy Res] 2007 Jun; Vol. 75 (1), pp. 46-51. Date of Electronic Publication: 2007 May 15. - Publication Year :
- 2007
-
Abstract
- We investigated the roles of mutations in voltage-gated sodium channel alpha 1 subunit gene (SCN1A) in epilepsies and psychiatric disorders. The SCN1A gene was screened for mutations in three unrelated Japanese families with generalized epilepsy with febrile seizure plus (GEFS+), febrile seizure with myoclonic seizures, or intractable childhood epilepsy with generalized tonic-clonic seizures (ICEGTC). In the family with GEFS+, one individual was affected with panic disorder and seizures, and another individual was diagnosed with Asperger syndrome and seizures. The novel mutation V1366I was found in all probands and patients with psychiatric disorders of the three families. These results suggest that SCN1A mutations may confer susceptibility to psychiatric disorders in addition to variable epileptic seizures. Unidentified modifiers may play critical roles in determining the ultimate phenotype of patients with sodium channel mutations.
- Subjects :
- Adult
Child
DNA Mutational Analysis
Epilepsy classification
Epilepsy complications
Female
Humans
Isoleucine genetics
Male
NAV1.1 Voltage-Gated Sodium Channel
Pedigree
Phenotype
Valine genetics
Epilepsy genetics
Genetic Predisposition to Disease
Mutation
Nerve Tissue Proteins genetics
Sodium Channels genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0920-1211
- Volume :
- 75
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Epilepsy research
- Publication Type :
- Academic Journal
- Accession number :
- 17507202
- Full Text :
- https://doi.org/10.1016/j.eplepsyres.2007.03.018