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Синдром AREDYLD

ORPHA:1133· ICD-10 Q87.8· AREDYLD syndrome

Визначення(English summary)

A rare genetic disease characterized by lipoatrophic diabetes, mild craniofacial dysmorphism (such as pronounced antitragal incisura and mandibular prognathism), ectodermal dysplasia (generalized hypotrichosis and dental and nail abnormalities), hypoplasia or aplasia of the breasts, and urogenital/renal anomalies. Additional reported manifestations include skeletal abnormalities and hepatosplenomegaly.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal recessive
Вік початку
Neonatal