Idiopathic renal hypouricemia: A case report and literature review

Idiopathic renal hypouricemia is a rare hereditary condition. Type 2 renal hyperuricemia (RHUC2) is caused by a mutation in the SLC2A9 gene, which encodes a high-capacity glucose and urate transporter, glucose transporter (GLUT)9. RHUC2 predisposes to exercise-induced acute renal failure (EIARF) and...

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Detalles Bibliográficos
Autores principales: Wang, Cuiyu, Wang, Jin, Liu, Song, Liang, Xinhua, Song, Yifan, Feng, Ling, Zhong, Lanxin, Guo, Xiaohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854582/
https://www.ncbi.nlm.nih.gov/pubmed/31638209
http://dx.doi.org/10.3892/mmr.2019.10726

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854582/
https://www.ncbi.nlm.nih.gov/pubmed/31638209
http://dx.doi.org/10.3892/mmr.2019.10726

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