Mowat-Wilson syndrome

Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome characterized by a distinct facial phenotype, intellectual disability, epilepsy, Hirschsprung disease (HSCR) and variable congenital malformations.

Also known as: Hirschsprung disease intellectual disability syndrome, Hirschsprung disease-intellectual disability syndrome, Mowat-Wilson syndrome, microcephaly, intellectual disability, and distinct facial featrues, with or without Hirschprung disease, Hirschsprung disease-mental retardation syndrome, MOWS, intellectual disability, microcephaly, and distinct facial features with or without Hirschsprung disease, mental retardation, microcephaly, and distinct facial features with or without Hirschsprung disease

9 clinical trials for this condition and its sub-types.