genetic
Mowat–Wilson syndrome
Mowat–Wilson is a rare disorder that was clinically delineated by David R. Mowat and Meredith J. Wilson in 1998. The condition affects both males and females, has been described in various countries and ethnic groups around the world, and occurs in approximately 1 in 50,000–100,000 births.
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Treatment
- ·Supportive care
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