Literature DB >> 25417683

Gout as a manifestation of familial juvenile hyperuricemic nephropathy.

Heather Spain1, Troy Plumb, Ted R Mikuls.   

Abstract

We report 2 cases of familial juvenile hyperuricemic nephropathy, a rare autosomal dominant disorder characterized by uromodulin gene mutations leading to hyperuricemia secondary to profound renal uric acid underexcretion, gout, and chronic renal disease. Case 1 involves a 56-year-old woman who underwent a kidney transplant after steady decline in kidney function since the age of 19 years. Her gout had been successfully controlled with varying doses of daily allopurinol. Case 2, the son of case 1, presented with already progressive and debilitating arthritis at the age of 34 years with relatively stable chronic renal failure that was also subsequently managed with daily allopurinol and judicious anti-inflammatory prophylaxis.

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Year:  2014        PMID: 25417683     DOI: 10.1097/RHU.0000000000000188

Source DB:  PubMed          Journal:  J Clin Rheumatol        ISSN: 1076-1608            Impact factor:   3.517


  1 in total

1.  A novel likely pathogenic variant in the UMOD gene in a family with autosomal dominant tubulointerstitial kidney disease: a case report.

Authors:  Ying Wang; Haibo Liu; Qingnan He; Zhuwen Yi; Yongzhen Li; Xiqiang Dang
Journal:  BMC Nephrol       Date:  2020-08-26       Impact factor: 2.388

  1 in total

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