Prader–Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes. In newborns, symptoms include weak muscles, poor feeding, and slow development.
The frequency set corresponds with Chromosome disorders frequencies
The set assists with symptoms of Prader–Willi syndrome
0.13, 0.35, 0.95, 0.50, 027.50, 352.93, 426.9
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