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Синдром Коффіна-Сіріса

ORPHA:1465· ICD-10 Q87.1· Coffin-Siris syndrome

Визначення(English summary)

A rare genetic syndromic intellectual disability of broad phenotypic range characterized by developmental delay and variable clinical features which most commonly, but not consistently, include aplasia or hypoplasia of the distal phalanx or nail of the fifth digit, and coarse facial features.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal dominant
Вік початку
Antenatal, Neonatal