Mowat-Wilson syndrome , MWS (Abkürzung)

All children with Mowat-Wilson syndrome required early intervention with speech therapy and physical therapy.

Mutations in the ZEB2 gene is associated with the Mowat-Wilson syndrome.

However, Hirschsprung's disease is not present in all infants with Mowat-Wilson syndrome and therefore it is not a required diagnostic criterion.

This includes Angelman syndrome, Mowat-Wilson syndrome and Rett syndrome.

Mowat-Wilson syndrome is caused by an abnormality in ZFHX1B gene that is usually the result of a new genetic change (mutation) in the affected person.

Hirschsprung's disease can also present as part of a syndrome in Waardenburg-Shah syndrome, Mowat-Wilson syndrome, Goldberg-Shpritzen megacolon syndrome, and congenital central hypoventilation syndrome.

MWS Hirschsprung Disease-Mental Retardation Syndrome None Mowat-Wilson syndrome (MWS) is a rare genetic disorder that may be apparent at birth or in the first year of life.

Some syndromes that frequently include ACC are Aicardi syndrome, Andermann syndrome, Shapiro syndrome, acrocallosal syndrome, septo-optic dysplasia (optic nerve hypoplasia), Mowat-Wilson syndrome and Menkes syndrome.