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Тяжка неонатальна енцефалопатія з мікроцефалією

ORPHA:209370· ICD-10 Q02· MECP2-related severe neonatal encephalopathy

Визначення(English summary)

Severe neonatal-onset encephalopathy with microcephaly is a rare monogenic disease with epilepsy characterized by neonatal-onset encephalopathy, microcephaly, severe developmental delay or absent development, breathing abnormalities (including central hypoventilation and/or respiratory insufficiency), intractable seizures, abnormal muscle tone and involuntary movements. Early death is usual.

Поширеність
<1 / 1 000 000
Успадкування
X-linked recessive
Вік початку
Infancy, Neonatal