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Sheeza Basharat
Sheeza Basharat2 months ago
Prader–Willi syndrome- Features

Prader–Willi syndrome- Features

Prader–Willi syndrome (PWS) is a genetic disorder caused by a loss of function of specific genes on chromosome 15. In newborns, symptoms include weak muscles, poor feeding, and slow development. Beginning in childhood, those affected become constantly hungry, which often leads to obesity and type 2 diabetes.

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