A case of renal hypouricemia due to T217M mutation in SLC22A12 incidentally associated with IgA nephropathy

A case of renal hypouricemia due to T217M mutation in SLC22A12 incidentally associated with IgA nephropathy

Key Clinical Message A T217M heterozygous mutation in the SLC22A12 gene caused renal hypouricemia; this patient with IgA nephropathy had no findings other than IgA nephropathy on renal biopsy. Hypouricemia was susceptible to oxidative stress, but IgA nephropathy in the patient with hypouricemia coul...

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Main Authors: Yoshimasa Sakurabu, Haruhito A. Uchida, Toshihisa Tahara, Tomohiko Asakawa, Haruka Yamasaki, Katsuyoshi Katayama, Shugo Okamoto, Yasuhiro Onishi, Natsumi Matsuoka‐Uchiyama, Keiko Tanaka, Hidemi Takeuchi, Kenji Tsuji, Ryoko Umebayashi, Yuki Ohashi, Kimiyoshi Ichida, Jun Wada
Format: Article
Language:English
Published: Wiley 2024-09-01
Series:Clinical Case Reports
Subjects:
IgA nephropathy
renal hypouricemia
steroid pulse therapy
urate transporter
Online Access:https://doi.org/10.1002/ccr3.9368
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