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Синдром Харрода

ORPHA:2115· ICD-10 Q87.8· Harrod syndrome

Визначення(English summary)

A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive.

Поширеність
<1 / 1 000 000
Вік початку
Infancy, Neonatal