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IgA nephropathy in a patient with 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 p. Y329fs mutation: a case report and review

Paper C Peer reviewed Observational

Key takeaways

This is a single-patient report of a kidney disease (IgA nephropathy) alongside a rare hormone-gene disorder. One case cannot prove the two conditions are connected.

Who did this work

Ying Guo (Sichuan University) · Hong Jian Xie (Sichuan University) · Wei Dai (Sichuan University) · Ting Liu (Sichuan University)

Source

Indexed paper · OpenAlex — CKD concept sweep (DB seed + weekly delta) · 2026-08-06
https://doi.org/10.1186/s12887-026-07487-x