Catalog
Prader-Willi syndrome
Link to WHO Definition
Prader-Willi syndrome – http://id.who.int/icd/entity/393773440
Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioural problems or severe psychiatric problems.