vitalwiki

Трисомія 12р

ORPHA:1699· ICD-10 Q92.3· Trisomy 12p syndrome

Визначення(English summary)

A partial autosomal trisomy characterized by developmental delay and intellectual disability, generalized hypotonia, postnatal growth retardation, variable brain and heart anomalies and dysmorphic features, including frontal bossing, round face, full cheeks, low-set ears, broad nasal bridge, short nose with anteverted nares, long philtrum, thin upper lip vermilion, and everted, thick lower lip. Unspecific associated congenital anomalies have also been reported.

Поширеність
<1 / 1 000 000
Успадкування
Not applicable, Unknown
Вік початку
Neonatal