Prader–Willi syndrome
Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In babies, symptoms include weak muscles, poor feeding, and slow development.
Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In babies, symptoms include weak muscles, poor feeding, and slow development.
Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In babies, symptoms include weak muscles, poor feeding, and slow development.
Source: Wikipedia "Prader–Willi syndrome" · CC BY-SA 4.0
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