Epilepsy of infancy with migrating focal seizures due to a novel homozygous mutation in KCNT1 gene: A case report.

James, Joe; Govindaraj, Geeta; Gafoor, V Abdul; Kumar, Vinod; Smita, B; Balaram, Neetha; Jose, James

James, Joe; Govindaraj, Geeta; Gafoor, V Abdul; Kumar, Vinod; Smita, B; Balaram, Neetha; Jose, James.

Afiliação

James J; Department of Neurology, Government Medical College Kozhikode, Kozhikode, Kerala, India.
Govindaraj G; Department of Pediatrics, Government Medical College Kozhikode, Kozhikode, Kerala, India.
Gafoor VA; Department of Neurology, Government Medical College Kozhikode, Kozhikode, Kerala, India.
Kumar V; Department of Pediatrics, Government Medical College Kozhikode, Kozhikode, Kerala, India.
Smita B; Department of Neurology, Government Medical College Kozhikode, Kozhikode, Kerala, India.
Balaram N; Department of Neurology, Government Medical College Kozhikode, Kozhikode, Kerala, India.
Jose J; Department of Neurology, Government Medical College Kozhikode, Kozhikode, Kerala, India. Electronic address: drjamesjose@gmail.com.

Seizure ; 106: 36-38, 2023 03.

Article em En | MEDLINE | ID: mdl-36746065

Assuntos

Epilepsia; Convulsões; Lactente; Humanos; Convulsões/genética; Epilepsia/genética; Mutação/genética; Eletroencefalografia; Canais de Potássio Ativados por Sódio/genética; Proteínas do Tecido Nervoso/genética

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Convulsões / Epilepsia Limite: Humans / Infant Idioma: En Revista: Seizure Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Índia País de publicação: Reino Unido

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google