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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Veröffentlicht in:	Curēus (Palo Alto, CA) CA), 2022-12, Vol.14 (12), p.e33164
Hauptverfasser:	Alan, Serdar, Vural, Sevde Nur, Aliefendioglu, Didem, Senbil, Nesrin
Format:	Artikel
Sprache:	eng
Schlagworte:	Neurology Pediatrics
Online-Zugang:	Volltext
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