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Clinical Features and Genetic Diversity of Primary Hyperoxaluria: A Case Series Analysis of Chinese Patients.

Key takeaways

Thirteen patients with a rare genetic kidney disease were reviewed. The study describes their symptoms and how the disease affected their kidneys. This is a small observational case series, so it shows a link between the genes and symptoms, not proof of cause.

Who did this work

Yuan Y · Li L · Wang X · Gao E · Xu F · Cheng Z · Cheng D · Ni X · Xie K · Shi Z · Zeng C · Liang S

Source

Article · PubMed, Nutritional supplements and CKD · 2026 Oct 15
https://pubmed.ncbi.nlm.nih.gov/42879353/