Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome

Orpha code: 457284OMIM code: 616362

Definicja

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by variable degrees of developmental delay and intellectual disability with poor or absent speech, hypotonia, hypoplastic or absent corpus callosum, and facial dysmorphism (such as long face, frontal bossing, hypertelorism, downslanting palpebral fissures, and tented upper lip). Additional reported features include microcephaly, seizures, gait ataxia, scoliosis, and syndactyly of fingers, among others.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
457284
Kod OMIM
616362
Kod ICD10
-
Kod ICD11
-

No additional description.

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