Mowat-Wilson Syndrome

Mowat-Wilson Syndrome

Mowat-Wilson syndrome is a rare genetic disorder caused by mutations in the ZEB2 gene. Individuals with Mowat-Wilson syndrome often exhibit distinctive facial features, intellectual disability, and various congenital anomalies. Mowat-Wilson syndrome is typically diagnosed through genetic testing and managed with a multidisciplinary approach involving medical specialists and supportive therapies.