Mowat–Wilson syndrome
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Mowat–Wilson syndrome is a rare genetic disorder that was clinically delineated by David R. Mowat and Meredith J. Wilson in 1998.[1][2] 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.[3]
Quick Facts Other names, Differential diagnosis ...
Mowat–Wilson syndrome | |
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Other names | Hirschsprung disease-intellectual disability syndrome |
Mowat–Wilson syndrome, clinical features of Patient 2 at age: (A) 1 year and 6 months; (B–C) 3 years and 5 months; (D–E) 8 years and 1 month. | |
Differential diagnosis | Smith Lemli Opitz syndrome, Angelman syndrome, Goldberg Shprintzen megacolon syndrome |
Treatment | Supportive care |
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