Trisomy 8q

Orpha code: 1752OMIM code:

Definicja

A partial autosomal trisomy characterized by developmental delay, intellectual disability, prenatal and postnatal growth retardation, congenital heart, genitourinary and skeletal anomalies, and dysmorphic facial features, including high and broad forehead, hypertelorism, upslanting palpebral fissures, broad nose, dysplastic and low set ears, micrognathia. Phenotypic features vary in relation to the duplication size.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Duplication 8q
Duplikacja 8q
Kod ORPHA
1752
Kod OMIM
-
Kod ICD10
Q92.2
Kod ICD11
LD41.70

No additional description.

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