A Study On Prader Willi Syndrome Essay
PRADER-WILLI SYNDROME 2
Prader-Willi Syndrome is a congenital disorder as a result of a partial chromosome, having a missing segment when the child is gaining chromosomes; it creates an impact on the infant 's physically, mentally, and behaviorally. It is a defect on their chromosome 15, which affects one out of every 15000 births. Prader-Willi Syndrome (PWS) is a genetic disease that causes children to be hyperphagia meaning they never get full, along with abnormalities of their physical appearance, and if not diagnosed and treated early can lead to severe obesity.
Although there is no cure for this disease it can be managed with a group of health care professionals, and most importantly with the help of the child 's parents. The best way for it to be diagnosed is be a genetic test for specific markers in the child DNA. Along with a checklist of signs and symptoms as the child grows to properly diagnose this disease. It requires early diagnosis in order for the child to get treatment and be able to thrive with their life.
PRADER-WILLI SYNDROME 3
Prader-Willi syndrome, it is a disease that affects one in 15000 children, giving them an inability of controlling their own bodies in many ways. (Prader-Willi Syndrome). This disease is not one of the most popular or known but it still affects many people in our country. With an understanding of the disease it can be better treated for…