Trisomy 12p

Orpha code: 1699OMIM code:

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.

Disease data
Classification

Malformation syndrome

Synonyms
Duplication 12p
Duplikacja 12p
ORPHA code
1699
OMIM code
-
ICD10 code
Q92.3
ICD11 code
LD41.B1

No additional description.

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