Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome

Orpha code: 488627OMIM code: 617051

Definicja

A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by infantile onset of global developmental delay, severe intellectual disability, growth deficiency, microcephaly, strabismus, blue-gray sclerae, and extensive Mongolian spots. Some patients also present with epilepsy. Brain imaging may demonstrate variable abnormalities including cerebral atrophy, thin corpus callosum, ventriculomegaly, or arachnoid cysts.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
488627
Kod OMIM
617051
Kod ICD10
-
Kod ICD11
-

No additional description.

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