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Prader–Willi syndrome (abbreviated PWS) is a rare genetic disorder in which seven genes (or some subset thereof) on chromosome 15 (q 11–13) are deleted or Prader-Willi (PRAH-dur VIL-e) syndrome is a rare disorder present at birth that results in a number of physical, mental and behavioral problems. Prader-Willi syndrome Definition. Prader-Willi syndrome (PWS) is a genetic condition caused by the absence of chromosomal material from chromosome 15. Prader-Willi syndrome (PWS) is a genetic condition that affects many parts of the body. Infants with PWS have severe hypotonia (low muscle tone), feeding difficulties Prader-Willi Syndrome (PWS) What is Prader-Willi syndrome (PWS)? Prader-Willi syndrome (PWS) is a genetic syndrome that affects one in every 12,000-15,000 … Children with Prader-Willi syndrome have endocrine problems including reduced or absent secretion of sex hormones (hypogonadism) and delayed or incomplete sexual Background. Prader-Willi syndrome is a severely disabling genetic condition. Treatments are available, but there is no cure. Children aged up to 18 years may … 1 Prader-Willi Syndrome - Information Sheet 1 – to be included in the Personal Health Records of people who have a current problem with challenging behaviour  · Background. Prader-Willi (PWS) and Down Syndrome (DS) are two genetic disorders characterised by some common clinical and functional features. A Where can I find additional information about Prader-Willi syndrome? What other names do people use for Prader-Willi syndrome?