Prader

Prader
Andrea, Swiss pediatrician, *1919. See P.-Willi syndrome.

Medical dictionary. 2011.

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  • Prader — ist der Name von: Andrea Prader (1919–2001), Schweizer Kinderarzt und Endokrinologe Clemens Prader (* 1979), österreichischer Berufsgolfer Georg Prader (1917–1985), österreichischer Politiker der Österreichischen Volkspartei Georg Prader (CSP)… …   Deutsch Wikipedia

  • Prader–Willi syndrome — Prader Willi syndrome Classification and external resources ICD 10 Q87.1 ICD 9 759.81 …   Wikipedia

  • Prader-Willi, síndrome de — patol. Síndrome caracterizado por un conjunto de trastornos de movilidad (adinamia e hipotonía muscular), falta de desarrollo de los órganos genitales externos, una fuerte alteración del aspecto facial (estrabismo, frente prominente, malformación …   Diccionario médico

  • 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-Syndrom — Klassifikation nach ICD 10 Q87.1 Angeborene Fehlbildungssyndrome, die vorwiegend mit Kleinwuchs einhergehen (inkl.: Prader Willi Syndrom) …   Deutsch Wikipedia

  • Prader-Willy-Syndrom — Klassifikation nach ICD 10 Q87.1 Angeborene Fehlbildungssyndrome, die vorwiegend mit Kleinwuchs einhergehen (inkl.: Prader Willi Syndrom) …   Deutsch Wikipedia

  • 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 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

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