What Is Prader-Willi Syndrome?
What Is Prader-Willi Syndrome?
Prader-Willi Syndrome (PWS) is a rare genetic disorder that causes poor muscle tone (hypotonia) in infancy that leads to feeding issues, followed by a relentless hunger (hyperphagia) and severe obesity starting in early childhood, along with learning disabilities, short stature, and underdeveloped sex organs. It results from missing or inactive paternal genes on chromosome 15, affecting the brain's control of appetite and hormones. Last but not least, management and treatment of the disorder involves strict food control, growth hormone treatments, therapies like feeding, occupational, speech, and physical. As well as addressing behavioral challenges. Oh and as of now there's currently no cure, but research aims to manage the constant hunger that people with this disorder fact.
