Prader-Willi Syndrome
Einstein Health Glossary
ICD 10 - Q87.1
What is Prader-Willi Syndrome?
Associated with a defect on chromosome 15, Prader-Willi Syndrome is a genetic disorder that causes several symptoms.
Symptoms
The first symptoms of Prader-Willi Syndrome appear in childhood. Due to hormonal changes, it is comm.
Causes
Prader-Willi Syndrome is caused by a defect on chromosome 15 that leads to different changes in the b.
Diagnosis
The diagnosis of Prader-Willi Syndrome is based on a genetic test, along with certain physical and beha.
Prevention
There is no way to prevent Prader-Willi Syndrome.
Treatment
Prader-Willi Syndrome has no cure. Treatment varies according to the symptoms that most affect each.
Duration
Prader-Willi Syndrome is a lifelong condition.
Is it contagious?
Prader-Willi Syndrome is not contagious.
Can it be contracted more than once?
Prader-Willi Syndrome is only diagnosed once.