Trisomy 12p

Orpha code: 1699OMIM code:

Definicja

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.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Duplication 12p
Duplikacja 12p
Kod ORPHA
1699
Kod OMIM
-
Kod ICD10
Q92.3
Kod ICD11
LD41.B1

No additional description.

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