Prader-Willi Syndrome is a rare genetic disorder that occurs due to a defect in chromosome 15. It is characterised small hands and feet, small stature, hypotonia, intellectual disability and insatiable hunger which may lead to early onset obesity and extreme obesity.
Drugs used to treat Prader-Willi Syndrome
| Name | Drug Class |
|---|---|
| Omnitrope | Growth hormones |
| Genotropin | Growth hormones |
