In the year 2000 it was shown that the genetic deficiency in LNS could be corrected in vitro. A virus was used to insert a normal copy of the HPRT1 gene into deficient human cells. Such techniques used in gene therapy may one day provide a cure for this disease. For now, medications are used to decrease the levels of uric acid. (Source: Genes and Disease by the National Center for Biotechnology)
Some of the clinical trials for Lesch-Nyhan syndrome include:
Medical research papers related to Lesch-Nyhan syndrome include:
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