← Назад

Self-limited neonatal-infantile epilepsy

ORPHA:140927DiseaseAutosomal dominantInfancy, Neonatal

Ассоциированные гены (2)

SCN2A
sodium voltage-gated channel alpha subunit 2
Disease-causing germline mutation(s) in
OMIM: 182390
KCNQ2
potassium voltage-gated channel subfamily Q member 2
Disease-causing germline mutation(s) in
OMIM: 602235

Фенотипы (15)

Частый (30–79%)5
HP:0002069Bilateral tonic-clonic seizure
HP:0002266Focal clonic seizure
HP:0011193EEG with focal spikes
HP:0032792Tonic seizure
HP:0032807Neonatal seizure
Периодический (5–29%)8
HP:0001350Slurred speech
HP:0002018Nausea
HP:0002104Apnea
HP:0002131Episodic ataxia
HP:0002172Postural instability
HP:0002315Headache
HP:0002321Vertigo
HP:0025401Staring gaze
Очень редкий (1–4%)2
HP:0001268Mental deterioration
HP:0031491Continuous spike and waves during slow sleep

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы