Prader-Willi Syndrome: Symptoms, Causes, and Treatment

What Is Prader-Willi Syndrome?

Prader-Willi syndrome is a rare genetic disease that occurs due to the mutation in chromosome 15. It affects various parts of the body. It is named after Andrea Prader and Heinrich Willi, the first people who diagnosed the condition. The symptoms of Prader-Willi may differ for each person. One of the most common features of the condition is overeating, which usually starts sometime in the toddler years. The syndrome may also disrupt a person’s mood and behavior, and their physical and intellectual development.

Studies show that 1 in 10,000 to 30,000 people are born with Prader-Willis syndrome every year. Studies also show that about 10,000 to 20,000 people live with the condition in the United States. There is no permanent cure for the condition. However, proper treatment can improve your quality of life and reduce your risk of developing medical complications.

In this article, we will discuss some important things to note about Prader-Willi syndrome, such as the symptoms, causes, treatment, and more.