A Case of Early Infantile Epileptic Encephalopathy Due to KCNQ2 Gene Mutation Presenting With Episodes of Hiccups

Neonatal epilepsy syndromes are responsible for only 15% of the cases of neonatal seizure. An underlying genetic disorder can be detected in approximately 42% of this subgroup. KCNQ2 gene-associated epilepsies are very rare and more common presentations are self-limited familial neonatal epilepsy (S...

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Detalles Bibliográficos
Autores principales: Alan, Serdar, Vural, Sevde Nur, Aliefendioglu, Didem, Senbil, Nesrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885515/
https://www.ncbi.nlm.nih.gov/pubmed/36726904
http://dx.doi.org/10.7759/cureus.33164

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885515/
https://www.ncbi.nlm.nih.gov/pubmed/36726904
http://dx.doi.org/10.7759/cureus.33164

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