Hereditary renal hypouricemia with SLC22A12 mutation: A case report

Pediatr Neonatol. 2022 Mar;63(2):202-203. doi: 10.1016/j.pedneo.2021.08.012. Epub 2021 Oct 14.

Authors

Jisook Yim¹, Myungshin Kim¹, Jin-Soon Suh²

Affiliations

¹ Department of Laboratory Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
² Department of Pediatrics, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea. Electronic address: rebekahjs@catholic.ac.kr.

PMID: 34756726
DOI: 10.1016/j.pedneo.2021.08.012

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Humans
Mutation
Organic Anion Transporters* / genetics
Organic Cation Transport Proteins / genetics
Renal Tubular Transport, Inborn Errors* / genetics
Urinary Calculi* / genetics

Substances

Organic Anion Transporters
Organic Cation Transport Proteins
SLC22A12 protein, human

Supplementary concepts

Renal hypouricemia