Lesch–Nyhan syndrome — Lesch Nyhan syndrome Classification and external resources ICD 10 E79.1 ICD 9 277.2 … Wikipedia
Lesch-Nyhan syndrome — Lesch Ny·han syndrome lesh nī ən n a rare and usu. fatal genetic disorder of male children that is inherited as an X linked recessive trait and is characterized by hyperuricemia, mental retardation, spasticity, compulsive biting of the lips and… … Medical dictionary
Lesch-Nyhan syndrome — Lesch Nyhan syndrome. См. синдром Леша Найхана. (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.
Lesch-Nyhan syndrome — Infobox Disease Name = Lesch Nyhan syndrome Caption = Philip Baker, an adult with Lesch Nyhan Syndrome. Visible in this picture are the restraints on Philip s chair that he must use to control his involuntary movement. ICD10 = ICD10|E|79|1|e|70… … Wikipedia
lesch-nyhan syndrome — ¦leshˈnīən noun also lesch nyhan disease Usage: usually capitalized L&N Etymology: after Michael Lesch b1939 American cardiologist and William L. Nyhan b1926 American pediatrician : a rare and usually fatal genetic disorder of male children that… … Useful english dictionary
Lesch-Nyhan syndrome — A sex linked recessive inherited disease in humans that results from mutation in the gene for the purine salvage enzyme HGPRT, located on the X chromosome. Results in severe mental retardation and distressing behavioural abnormalities, such as… … Dictionary of molecular biology
Lesch-Nyhan syndrome — noun A rare inherited genetic disorder, caused by a deficiency of HGPRT, in which uric acid builds up in all body fluids … Wiktionary
Lesch - Nyhan syndrome — … Useful english dictionary
Syndrome de lesch-nyhan — Autre nom Déficit en hypoxanthine guanine phosphoribosyltransférase Référence MIM … Wikipédia en Français
Lesch-Nyhan-Syndrom — Klassifikation nach ICD 10 E79.1 Lesch Nyhan Syndrom … Deutsch Wikipedia
