What is Prader-Willi Syndrome?
Prader-Willi syndrome is a rare genetic condition that affects around 1 in 15,000 babies born in the United States alone.
Symptoms of Prader-Willi include chronic overeating, constant hunger, intellectual impairment, and behavioral issues.
In infants, symptoms also include slower development and weak muscle tone.
Is there a cure for Prader-Willi?
Currently, there is no cure for Prader-Willi syndrome. However, with the help of growth hormones and a modified diet, Prader-Willi can be somewhat controlled.
However, the costs of a specialized diet, as well as the doctor visits and medicines can become quite costly.
What is Prader-Willi Syndrome?
Prader-Willi syndrome is a rare genetic condition that affects around 1 in 15,000 babies born in the United States alone.
Symptoms of Prader-Willi include chronic overeating, constant hunger, intellectual impairment, and behavioral issues.
In infants, symptoms also include slower development and weak muscle tone.
Is there a cure for Prader-Willi?
Currently, there is no cure for Prader-Willi syndrome. However, with the help of growth hormones and a modified diet, Prader-Willi can be somewhat controlled.
However, the costs of a specialized diet, as well as the doctor visits and medicines can become quite costly.