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

Orpha code: 488627OMIM code: 617051

Definition

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
Classification

Malformation syndrome

ORPHA code
488627
OMIM code
617051
ICD10 code
-
ICD11 code
-

No additional description.

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