Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome

Orpha code: 513456OMIM code: 617616

Definicja

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay, intellectual disability, seizures, abnormal gait, and craniofacial dysmorphism (including coarse features, depressed nasal bridge, anteverted nares, broad nasal tip, prominent maxilla and upper lip, wide mouth, abnormal gingiva, and widely spaced teeth). Additional reported manifestations are ocular anomalies, cardiac defects, gastrointestinal problems, and autistic features. Brain imaging may show thin corpus callosum, white matter abnormalities, or dilated ventricles.

Disease data
Klasyfikacja

Disease

Synonimy
Skraban-Deardorff syndrome
zespół Skraban i Deardorffa
Kod ORPHA
513456
Kod OMIM
617616
Kod ICD10
-
Kod ICD11
-

No additional description.

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