Warsaw breakage syndrome

Orpha code: 280558OMIM code: 613398

Definicja

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by pre- and postnatal growth restriction, microcephaly, mild to severe intellectual disability, sensorineural hearing loss with cochlear abnormalities, and facial dysmorphism (with small and elongated face, bifrontal narrowing, epicanthus, short nose, small nares, dysplastic ears, and short neck). Additional variable features include limb malformations, cardiac anomalies, abnormal skin pigmentation, and recurrent infections, among others.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
WABS
WABS
Kod ORPHA
280558
Kod OMIM
613398
Kod ICD10
Q87.8
Kod ICD11
LD2F.1Y

No additional description.

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