Lesch-Nyhan Disease - PubMed
Lesch-Nyhan Disease
William L Nyhan. J Hist Neurosci. 2005 Mar.
Abstract
The first description of Lesch-Nyhan disease was in 1964; the first two patients were seen in 1963. The disease has caught the imagination of a variety of clinicians and scientists. The clinical picture is striking, combining spasticity, involuntary movements, and cognitive retardation with self-injurious behavior and the manifestations of gout. Biochemically, the overproduction of uric acid--the end product of purine metabolism--was, when measured, the largest ever seen. The disease is now well understood on a molecular basis. Enzyme analysis and mutational analysis have made available a full range of genetic testing, including diagnosis, carrier detection, and prenatal diagnosis. Therapy with allopurinol has been effective for those manifestations the disease shares with gout. Treatment for the neurological and behavioral features of the disease remains elusive.
Similar articles
-
Update on the phenotypic spectrum of Lesch-Nyhan disease and its attenuated variants.
Torres RJ, Puig JG, Jinnah HA. Torres RJ, et al. Curr Rheumatol Rep. 2012 Apr;14(2):189-94. doi: 10.1007/s11926-011-0231-5. Curr Rheumatol Rep. 2012. PMID: 22198833 Free PMC article. Review.
-
Genotypic and phenotypic spectrum in attenuated variants of Lesch-Nyhan disease.
Fu R, Chen CJ, Jinnah HA. Fu R, et al. Mol Genet Metab. 2014 Aug;112(4):280-5. doi: 10.1016/j.ymgme.2014.05.012. Epub 2014 May 28. Mol Genet Metab. 2014. PMID: 24930028 Free PMC article. Review.
-
Ambarsari CG, Cahyadi D, Sari L, Satria O, Sahli F, Darmadi TL, Kadaristiana A. Ambarsari CG, et al. Ren Fail. 2020 Nov;42(1):113-121. doi: 10.1080/0886022X.2020.1713805. Ren Fail. 2020. PMID: 31985336 Free PMC article.
-
The diagnosis of HPRT deficiency in the 21st century.
Torres RJ, Puig JG. Torres RJ, et al. Nucleosides Nucleotides Nucleic Acids. 2008 Jun;27(6):564-9. doi: 10.1080/15257770802135778. Nucleosides Nucleotides Nucleic Acids. 2008. PMID: 18600505
-
Hypoxanthine-guanine phosophoribosyltransferase (HPRT) deficiency: Lesch-Nyhan syndrome.
Torres RJ, Puig JG. Torres RJ, et al. Orphanet J Rare Dis. 2007 Dec 8;2:48. doi: 10.1186/1750-1172-2-48. Orphanet J Rare Dis. 2007. PMID: 18067674 Free PMC article. Review.
Cited by
-
Reisz JA, Dzieciatkowska M, Stephenson D, Gamboni F, Morton DH, D'Alessandro A. Reisz JA, et al. Antioxidants (Basel). 2023 Aug 31;12(9):1699. doi: 10.3390/antiox12091699. Antioxidants (Basel). 2023. PMID: 37760001 Free PMC article.
-
Kopra K, Mahran R, Yli-Hollo T, Tabata S, Vuorinen E, Fujii Y, Vuorinen I, Ogawa-Iio A, Hirayama A, Soga T, Sasaki AT, Härmä H. Kopra K, et al. Anal Bioanal Chem. 2023 Nov;415(27):6689-6700. doi: 10.1007/s00216-023-04944-9. Epub 2023 Sep 16. Anal Bioanal Chem. 2023. PMID: 37714971 Free PMC article.
-
Genital self-mutilation: A challenging pathology (Review).
Lupu S, Bratu OG, Tit DM, Bungau S, Maghiar O, Maghiar TA, Scarneciu CC, Scarneciu I. Lupu S, et al. Exp Ther Med. 2021 Oct;22(4):1130. doi: 10.3892/etm.2021.10564. Epub 2021 Aug 5. Exp Ther Med. 2021. PMID: 34504580 Free PMC article. Review.
-
Assessment and Treatment of Self-Injurious Behavior Associated with Donnai-Barrow Syndrome.
Roane H, Bouxsein K, Fulton C. Roane H, et al. J Dev Phys Disabil. 2012 Aug;24(4):327-335. doi: 10.1007/s10882-012-9272-6. J Dev Phys Disabil. 2012. PMID: 25632217 Free PMC article.
-
Lesch-Nyhan Syndrome: Models, Theories, and Therapies.
Bell S, Kolobova I, Crapper L, Ernst C. Bell S, et al. Mol Syndromol. 2016 Nov;7(6):302-311. doi: 10.1159/000449296. Epub 2016 Sep 24. Mol Syndromol. 2016. PMID: 27920633 Free PMC article. Review.
Publication types
MeSH terms
Substances
Personal name as subject
LinkOut - more resources
Full Text Sources