Brain malformation-congenital heart disease-postaxial polydactyly syndrome

Orpha code: 75389OMIM code:

Definicja

A rare multiple congenital anomalies/dysmorphic syndrome characterized by intrauterine growth retardation, multiple congenital malformations (such as brain malformations including ectopic neuropituitary gland, hypoplastic adenopituitary, and hypoplastic cerebellar vermis, cardiac and renal anomalies, and postaxial polydactyly), abnormal hair structure with temporal balding, and dysmorphic facial features with hypoplastic nasal bridge, anteverted nostrils, dysplastic ears, long and smooth philtrum, narrow upper lip, and prominent, asymmetric lower lip. Postnatal growth retardation and severe developmental delay have also been reported.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Goossens-Devriendt syndrome
Zespół Goossensa i Devriendta
Kod ORPHA
75389
Kod OMIM
-
Kod ICD10
Q87.8
Kod ICD11
-

No additional description.

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