Prader-Willi Syndrome
Prader-Willi Syndrome (PWS) is a genetic disorder that occurs when a particular region of chromosome 15 is deleted or unexpressed when inherited from the father. It is characterized by weak muscle tone, short stature, cognitive disabilities, and an insatiable appetite that often leads to obesity. PWS is estimated to affect one in every 15,000 to 30,000 people. Early detection of PWS is essential for providing proper care, improved outcomes, and increased quality of life. Early diagnosis helps in providing timely interventions, such as diet and exercise support and behavior management, to prevent some of the most serious consequences associated with the disorder. Treatment plans may also include physical and occupational therapy, medical professionals to monitor and manage medical concerns, and genetic counseling.
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