| Literature DB >> 27764983 |
Kamila A Kaminska-Pajak1, Katarzyna Dyga2, Piotr Adamczyk3, Maria Szczepańska3, Marcin Zaniew4, Bodo Beck5, Marcin Tkaczyk1,6.
Abstract
Hyperuricemia is a common symptom in adult population. It usually accompanies the chronic kidney disease. Less frequently, it is a primary phenomenon causing later serious clinical consequences. Familial juvenile hyperuricemic nephropathy (FJHN) is one of the hereditary conditions associated with high levels of serum uric acid and leading to dialysis in young adult age. It results from mutation in the UMOD gene, encoding the uromodulin protein, that is, Tamm-Horsfall protein. The aim of this paper was to present two families (7 affected members) with FJHN, in whom standard nephrological diagnostics did not provide clear cause of dialysis-dependent chronic kidney disease, until genetic testing was performed.Entities:
Keywords: Hyperuricemia; children; familial juvenile hyperuricemic nephropathy; uromodulin
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Year: 2016 PMID: 27764983 DOI: 10.1080/0886022X.2016.1229991
Source DB: PubMed Journal: Ren Fail ISSN: 0886-022X Impact factor: 2.606