Medical Definition of Mowat-Wilson syndrome

Reviewed on 6/3/2021

Mowat-Wilson syndrome: a genetic (inherited) condition present at birth that features square-shaped face with deep-set, widely spaced eyes, a broad nasal bridge, pointed chin, uplifted earlobes, intellectual disability,the intestinal disorder Hirschsprung disease, small head (microcephaly), other birth defects, and delayed development and motor skills.

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NIH; Genetics Home Reference. Mowat-Wilson syndrome.
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