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Синдром 3М

ORPHA:2616· ICD-10 Q87.1· 3M syndrome

Визначення(English summary)

A rare primordial growth disorder characterized by low birth weight, reduced birth length, severe postnatal growth restriction, large head size, a spectrum of minor anomalies (including facial dysmorphism) and normal intelligence.

Поширеність
Unknown
Успадкування
Autosomal recessive
Вік початку
Antenatal