Epilepsy research · 2007
Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.
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Osaka Hitoshi, Ogiwara Ikuo, Mazaki Emi, Okamura Nami, Yamashita Sumimasa, Iai Mizue, Yamada Michiko, Kurosawa Kenji, Iwamoto Hiroko, Yasui-Furukori Norio, Kaneko Sunao, Fujiwara Tateki, Inoue Yushi, Yamakawa Kazuhiro
Аннотация
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.