Citation, DOI & article data
Mowat-Wilson syndrome is a rare disorder with a broad spectrum of congenital anomalies. It is caused by an abnormality in the ZFHX1B gene. Anomalies that may be recognized at birth or 1st year of life include:
- 1. Mowat-Wilson Syndrome - NORD (National Organization for Rare Disorders). NORD (National Organization for Rare Disorders).