Hypouricemia with recurrent nephrolithiasis: an overlooked entity: Answers

Pediatr Nephrol. 2023 Oct;38(10):3283-3284. doi: 10.1007/s00467-023-06003-y. Epub 2023 May 4.

Authors

Zehra Aydin¹, Huseyin Bilgin², Ceyda Cilasun³, Ilyas Halil Aydin⁴

Affiliations

¹ Department of Nephrology, Batman Training and Research Hospital, Batman, Turkey. zehraydn@hotmail.com.
² Department of Pediatric Metabolism and Nutrition, Diyarbakir Children's Hospital, Diyarbakir, Turkey.
³ Department of Pediatric Metabolism and Nutrition, Ankara Bilkent City Hospital, Ankara, Turkey.
⁴ Department of Pediatric Surgery, Ankara Etlik City Hospital, Ankara, Turkey.

PMID: 37140710
DOI: 10.1007/s00467-023-06003-y

No abstract available

Keywords: Child; Hereditary xanthinuria; MOCOS gene; Uric acid.

MeSH terms

Humans
Nephrolithiasis* / complications
Purine-Pyrimidine Metabolism, Inborn Errors*