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Lesch–Nyhan syndrome
Lesch–Nyhan syndrome (LNS), also known as Nyhan's syndrome, Kelley-Seegmiller syndrome and Juvenile gout, is a rare inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT), produced by mutations in the HPRT gene.
Lesch–Nyhan syndromeJ. Edwin SeegmillerUric acidGoutList of genetic disordersWilliam NyhanMichael LeschBiteThe Cobra EventHypoxanthine-guanine phosphoribosyltransferaseChoreoathetosisInborn errors of purine-pyrimidine metabolismLNSOxidopamineCoprolaliaThe Jerk (House)Self-harmList of geneticistsTourette syndromeNyhan
Pro-oxidantList of ICD-9 codes 240-279: endocrine, nutritional and metabolic diseases, and immunity disordersChorea gravidarumX-linked recessive inheritanceDeep brain stimulationList of acronyms for diseases and disordersHyperuricemiaAsymptomaticICD-10 Chapter IV: Endocrine, nutritional and metabolic diseasesInborn error of metabolismBasal ganglia diseaseUC San Diego School of MedicinePica (disorder)Werner CatelNucleotide salvagePurine metabolismDermatophagiaMartin EvansNip/Tuck (season 6)
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