Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome

Orpha code: 513456OMIM code: 617616

Definition

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
Classification

Disease

Synonyms
Skraban-Deardorff syndrome
zespół Skraban i Deardorffa
ORPHA code
513456
OMIM code
617616
ICD10 code
-
ICD11 code
-

No additional description.

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