- hypotonia), excess appetite that if unchecked leads to obesity, small hands and feet and mental retardation. The syndrome is due to the lack in the child of chromosome region 15q11-13 from their father. The child may have two copies of chromosome region 15q11-13 from their mother (a phenomenon called maternal disomy). Although candidate genes in 15q11-13 have been identified, the exact gene or genes that give rise to the syndrome are not known. There is currently no specific treatment or cure for Prader-Willi syndrome. Parents are advised to limit consumption of high-calorie foods, and to use techniques such as special education, speech therapy, and physical therapy to maximize the child’s potential. In some cases, antidepressant or stimulant medication is tried, which may effect appetite, attention, and behavior. Severe psychiatric illness is common in Prader-Willi adults. Those with psychotic illness have a double maternal copy of 15q11-13, suggesting that genes in this region are important in causing psychotic illness.
Medical dictionary. 2011.
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Prader–Willi syndrome — Prader Willi syndrome Classification and external resources ICD 10 Q87.1 ICD 9 759.81 … Wikipedia
Syndrome de prader-willi — Autre nom Syndrome de Prader Labhart Willi Référence MIM … Wikipédia en Français
Syndrome de Prader-Willi — Classification et ressources externes CIM 10 Q87.1 CIM 9 759.81 OMIM … Wikipédia en Français
Prader-Willi syndrome — Prader Willi Labhart syndrome a congenital condition that is inherited as an autosomal dominant trait and is due to an abnormality of chromosome 15 (see imprinting). It is marked by pathological overeating and resulting obesity (affected children … The new mediacal dictionary
Prader-Willi syndrome — Prader Willi syndrome. См. синдром Прадера Вилли. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
Prader-Willi-Labhart syndrome — Prader Willi syndrome … The new mediacal dictionary
Prader-Willi syndrome — Infobox Disease Name = Prader Willi syndrome Caption = DiseasesDB = 10481 ICD10 = ICD10|Q|87|1|q|80 ICD9 = ICD9|759.81 ICDO = OMIM = 176270 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1880 MeshID = D011218 Prader Willi syndrome… … Wikipedia
Prader-Willi-Syndrom — Klassifikation nach ICD 10 Q87.1 Angeborene Fehlbildungssyndrome, die vorwiegend mit Kleinwuchs einhergehen (inkl.: Prader Willi Syndrom) … Deutsch Wikipedia
Prader-Willi syndrome — A condition characterized by muscle floppiness (hypotonia), excess appetite that if unchecked leads to obesity, small hands and feet and mental retardation. The syndrome is due to the lack in the child of chromosome region 15q11 13 from their… … Medical dictionary
prader-willi syndrome — ˈprädə(r)ˈvilē noun Usage: usually capitalized P&W Etymology: after Andrea Prader b1919 and Heinrich Willi died 1971 Swiss pediatricians : a genetic disorder characterized by short stature, mental retardation, hypotonia, abnormally small hands… … Useful english dictionary