There is no cure for Prader-Willi syndrome as of 2015; however, doctors can treat its symptoms with growth hormones; sex hormone replacement; sleep monitoring; and speech, language, physical and behavioral therapies, notes Everyday Health. Parents can also help prevent complications from Prader-Willi syndrome by monitoring their children's food intake.Continue Reading
Prader-Willi syndrome is a rare genetic disease that is present at birth and causes several physical, neurological, cognitive and behavioral problems, states Everyday Health. Children with the disorder suffer from various symptoms, such as behavioral issues, delayed motor development, underdeveloped genitals and constant hunger. Growth hormones can help with poor muscle tone in babies and can improve physical strength, muscle mass and bone density. Since people with Prader-Willi syndrome often never feel full, supervision of food intake is important to prevent obesity and diabetes.
People who have Prader-Willi syndrome are also at risk of congestive heart failure, osteoporosis and other bone conditions, according to Everyday Health. Because the syndrome occurs randomly, there are no specific risk factors for being born with the condition. The genetic error present in the syndrome occurs on chromosome 15, and doctors have pinpointed lack of paternal genes on this chromosome, two genes from mothers and none from fathers and paternal genes that are inactive as contributors to the development of Prader-Willi.Learn more about Conditions & Diseases