Thelansis

  Prader–Willi syndrome is a genetic disorder due to the loss of function of specific genes. In newborns, symptoms include weak muscles, poor feeding, and slow development. Beginning in childhood, the person becomes constantly hungry, which often leads to obesity and T2D. ·        Patients with Prader-Willi syndrome frequently reach adulthood and are able to function in a group home setting, performing vocational work, or attending community college classes. Diminished sensitivity to pain and diminished capacity to vomit may delay the diagnosis of underlying disease ·        According to Thelansis’s research prevalence at birth is estimated at 1/15,000-30,000 worldwide. Most estimates place the incidence between 1 in 10,000-30,000 individuals in the general population and about 350,000-400,000 individuals worldwide. PWS affects males and females in equal numbers and occurs in all ethnic groups and geographic regions in...