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Trisomy 12p syndrome

ORPHA:1699· ICD-10 Q92.3

Definition

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.

Prevalence
<1 / 1 000 000
Inheritance
Not applicable, Unknown
Age of onset
Neonatal