Brain malformation-congenital heart disease-postaxial polydactyly syndrome

Orpha code: 75389OMIM code:

Definition

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
Classification

Malformation syndrome

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

No additional description.

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