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The Lowest Uric Acid in Kidney Transplant and Review of Literature

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Date 2023 Jun 29
PMID 37383421
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Abstract

Heredity hypouricemia is caused by renal hypouricemia or xanthinuria. Xanthinuria is divided into type 1 with deficiency of xanthine dehydrogenase and type 2 with xanthine dehydrogenase and aldehyde oxidase deficiency. We report a case of xanthinuria type 1 that developed with kidney failure. Hemodialysis was done for him, but kidney function was not improved, so a kidney transplant was performed for him. His serum uric acid was 0.1 mg/dl before and after transplantation.

References
1.
Iguchi A, Sato T, Yamazaki M, Tasaki K, Suzuki Y, Iino N . A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase. CEN Case Rep. 2017; 5(2):158-162. PMC: 5413754. DOI: 10.1007/s13730-016-0216-3. View

2.
Kim H, Ihm C, Jeong K, Kang H, Kim J, Lim H . A Case Report of Familial Renal Hypouricemia Confirmed by Genotyping of SLC22A12, and a Literature Review. Electrolyte Blood Press. 2016; 13(2):52-7. PMC: 4737662. DOI: 10.5049/EBP.2015.13.2.52. View

3.
Greene M, Marcus R, Aurbach G, Kazam E, Seegmiller J . Hypouricemia due to isolated renal tubular defect. Dalmatian dog mutation in man. Am J Med. 1972; 53(3):361-7. DOI: 10.1016/0002-9343(72)90181-7. View

4.
Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O . Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria. J Clin Invest. 1997; 99(10):2391-7. PMC: 508078. DOI: 10.1172/JCI119421. View

5.
Gok F, Ichida K, Topaloglu R . Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria. Nephrol Dial Transplant. 2003; 18(11):2278-83. DOI: 10.1093/ndt/gfg385. View