Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders > Inherited > Lesch-Nyhan Syndrome
A rare, genetic disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase or HPRT.
http://www.ninds.nih.gov/disorders/lesch_nyhan/lesch_nyhan.htm
Information sheet compiled by the National Institute of Neurological Disorders and Stroke.
http://patient.info/doctor/lesch-nyhan-syndrome
Description, pathophysiology, epidemiology, presentation, investigations, differential diagnosis, management, complications, prognosis, prevention and history.
Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders > Inherited > Lesch-Nyhan Syndrome
Thanks to DMOZ, which built a great web directory for nearly two decades and freely shared it with the web. About us