Prader-Willi Syndrome
Prader-Willi syndrome is a congenital (present from birth) disease that involves obesity, decreased muscle tone, decreased mental capacity, and sex glands that produce little or no hormones... More »
healthline.com
... Prader-Willi syndrome is a congenital (present from birth) disease characterized by obesity , decreased muscle tone , decreased mental capacity, and hypogonadism .
www.nlm.nih.gov/medlineplus/ency/article/001605.htm#Def... www.nlm.nih.gov/medlineplus/ency/article/001605.htm#Definition
Prader-Willi Syndrome (PWS) is an uncommon genetic disorder. It causes poor muscle tone, low levels of sex hormones and a constant feeling of hunger. The part of the brain that controls feelings of fullness or hunger does not work properly in people with PWS. They overeat, leading to obesity.
www.nlm.nih.gov/medlineplus/praderwillisyndrome.html www.nlm.nih.gov/medlineplus/praderwillisyndrome.html
PWSA (USA) is an organization of families and professionals working together to promote and fund research, provide education, and offer support to enhance the quality of life of those affected by Prader-Willi syndrome.
www.pwsausa.org/
Q: What is Prader-Willi syndrome (PWS)? ... A: It is estimated that one in 12,000 to 15,000 people has PWS. Although considered a "rare" disorder, Prader-Willi syndrome is one of the most common conditions seen in genetics clinics and is the most common genetic cause of obesity that has been identified.
www.pwsausa.org/faq.htm
Prader-Willi syndrome - Wikipedia, the free encyclopedia
| DiseasesDB = 10481 | ICD10 = Q87.1 | ICD9 = 759.81 | ICDO = | OMIM = 176270| MedlinePlus = | eMedicineSubj = ped | eMedicineTopic = 1880 | MeshID = D011218 | }} Prader-Willi syndrome (abbreviated ...
en.wikipedia.org/wiki/Prader-Willi_syndrome
Prader-Willi syndrome (PWS), a genetic disorder that usually involves chromosome 15, is the most common form of obesity caused by a genetic syndrome. Diagnosis often is delayed until early childhood because the clinical findings are relatively nonspecific, particularly in infancy, and the dysmorphism often is subtle.1,2...
www.aafp.org/afp/20050901/827.html
Prader-Willi syndrome is a complex genetic condition that affects many parts of the body. In infancy, this condition is characterized by weak muscle tone (hypotonia), feeding difficulties, poor growth, and delayed development. Beginning in ...
http://www.medicinenet.com/prader-willi_syndrome/articl...
Symptoms of Prader-Willi syndrome including 43 medical symptoms and signs of Prader-Willi syndrome, alternative diagnoses, misdiagnosis, and correct diagnosis for Prader-Willi syndrome signs or Prader-Willi syndrome symptoms. ... Complications of Prader-Willi syndrome...
www.wrongdiagnosis.com/p/prader_willi_syndrome/symptoms... www.wrongdiagnosis.com/p/prader_willi_syndrome/symptoms.htm