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ORPHA:235· ICD-10 Q87.1· Dubowitz syndrome

Визначення(English summary)

Dubowitz syndrome (DS) is a rare multiple congenital syndrome characterized primarly by growth retardation, microcephaly, distinctive facial dysmorphism, cutaneous eczema, a mild to severe intellectual deficit and genital abnormalities.

Поширеність
Unknown
Успадкування
Autosomal recessive
Вік початку
Antenatal, Neonatal