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.