This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Case Reports

. 2009 May;24(5):1089-90.

doi: 10.1007/s00467-008-1081-x. Epub 2008 Dec 19.

Chronic peritoneal dialysis in a 4-year-old boy with Lesch-Nyhan disease

Su Jin Kim, Young Bae Sohn, Sung Won Park, Dong-Kyu Jin, Kyung Hoon Paik

PMID: 19096880
DOI: 10.1007/s00467-008-1081-x

Case Reports

Chronic peritoneal dialysis in a 4-year-old boy with Lesch-Nyhan disease

Su Jin Kim et al. Pediatr Nephrol. 2009 May.

. 2009 May;24(5):1089-90.

doi: 10.1007/s00467-008-1081-x. Epub 2008 Dec 19.

Authors

Su Jin Kim, Young Bae Sohn, Sung Won Park, Dong-Kyu Jin, Kyung Hoon Paik

PMID: 19096880
DOI: 10.1007/s00467-008-1081-x

No abstract available

PubMed Disclaimer

Similar articles

Novel HGPRT 293 A>G point mutation presenting as neonatal acute renal failure.
Wong H, Feber J, Chakraborty P, Drukker A, Filler G. Wong H, et al. Pediatr Nephrol. 2008 Feb;23(2):317-21. doi: 10.1007/s00467-007-0612-1. Epub 2007 Oct 13. Pediatr Nephrol. 2008. PMID: 17934765
Late diagnosis of Lesch-Nyhan disease variant.
Doucet BP, Jegatheesan D, Burke J. Doucet BP, et al. BMJ Case Rep. 2013 Dec 10;2013:bcr2013201997. doi: 10.1136/bcr-2013-201997. BMJ Case Rep. 2013. PMID: 24326440 Free PMC article.
Kelley-Seegmiller syndrome in a patient with complete hypoxanthine-guanine phosphoribosyltransferase deficiency.
Cossu A, Micheli V, Jacomelli G, Carcassi A. Cossu A, et al. Clin Exp Rheumatol. 2002 Nov-Dec;20(6):851-3. Clin Exp Rheumatol. 2002. PMID: 12508781
Inherited deficiency of hypoxanthine-guanine phosphoribosyltransferase in X-linked uric aciduria (the Lesch-Nyhan syndrome and its variants).
Seegmiller JE. Seegmiller JE. Adv Hum Genet. 1976;6:75-163. doi: 10.1007/978-1-4615-8264-9_2. Adv Hum Genet. 1976. PMID: 779428 Review. No abstract available.
Lesch-Nyhan syndrome: mutation, prevention, and therapy.
Caskey CT. Caskey CT. Res Publ Assoc Res Nerv Ment Dis. 1987;65:187-94. Res Publ Assoc Res Nerv Ment Dis. 1987. PMID: 3330841 Review. No abstract available.

See all similar articles

Cited by

Late diagnosis of Lesch-Nyhan disease complicated with end-stage renal disease and tophi burst: a case report.
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.
Genotype-phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder.
Fu R, Ceballos-Picot I, Torres RJ, Larovere LE, Yamada Y, Nguyen KV, Hegde M, Visser JE, Schretlen DJ, Nyhan WL, Puig JG, O'Neill PJ, Jinnah HA; Lesch-Nyhan Disease International Study Group. Fu R, et al. Brain. 2014 May;137(Pt 5):1282-303. doi: 10.1093/brain/awt202. Epub 2013 Aug 22. Brain. 2014. PMID: 23975452 Free PMC article. Review.

References

1. Med Hypotheses. 2004;63(1):131-4 - PubMed
1. Brain. 2006 May;129(Pt 5):1201-17 - PubMed
1. Pediatr Nephrol. 2006 Jul;21(7):1045-7 - PubMed
1. Pediatr Nephrol. 2007 Nov;22(11):1975-8 - PubMed

Publication types

Actions
Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Ovid Technologies, Inc.
- Springer