Epilepsy with a de novo missense mutation in the sodium channel a1 subunit: a case report.

Article Details

Citation

Stefanaki E, Aggelakou V, Orfanou M, Kokori E, Boutoufianakis S

Epilepsy with a de novo missense mutation in the sodium channel a1 subunit: a case report.

Acta Paediatr. 2006 Dec;95(12):1703-6.

PubMed ID
17129991 [ View in PubMed
]
Abstract

Most epilepsies are characterized as "idiopathic" because of the lack of a known cause. Nevertheless, recently, there has been significant progress in the molecular genetics of idiopathic epilepsy. Mutations in gene-encoding ion channels were found to be the underlying disorder in all idiopathic epilepsies with a known molecular basis. Missense mutations in the voltage-gated sodium channel a1 subunit gene (SCN1A) were firstly identified in patients with generalized epilepsy with febrile seizures plus additional symptoms (GEFS + ). Subsequently, mutations of SCN1A were also found in patients with severe myoclonic epilepsy of infancy (SMEI) or Dravet syndrome, and in patients with borderline SMEI (SMEB), a milder form of Dravet syndrome. We describe a case of a new missense de novo mutation of SCN1A in a child with the clinical features of borderline SMEI syndrome.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Sodium channel protein type 1 subunit alphaP35498Details