Prader Willi Syndrome

What is Prader Willi Syndrome?

Prader Willi syndrome is a rare genetic (inborn) disorder. It is characterized primarily by compulsive eating, mental retardation, and obesity. Secondary characteristics include hypotonia (low muscle tone), slow metabolic rate, small/undeveloped penis/testis, round face, almond shaped eyes, nervous picking of skin, and stubbornness. Prader Willi syndrom is not curable, but its symptoms are managed through diet and exercise.

Links to information about Prader Willi

Prader Willi Foundation, Inc. - provides information and services to all with an interest in Prader Willi syndrome, a rare genetic disorder.
Prader Willi Syndrome Association - dedicated to educating and assisting individuals and their families with PWS.
Arizona Chapter - with personal stories of families, picture of person with PWS, information about Prader Willi Syndrome
Genline - Prader Willi Syndrome
OMIM - Prader Willi Syndrome
Prader Willi Syndrome
FAQ - Prader Willi Syndrome
Prader-Willi Syndrome Arizona Association - with personal stories of families, picture of person with PWS, information about Prader Willi Syndrome.
Prader Willi Syndrome Association - dedicated to educating and assisting individuals and their families with PWS.