Recovery From Dialysis in Patients With Primary Hyperoxaluria Type 1 Treated With Pyridoxine: A Report of 3 Cases

Primary hyperoxaluria type 1 (PH1) is a genetic disorder characterized by overproduction of oxalate and eventual kidney failure. Kidney failure is usually irreversible in PH1. However, in PH1 patients homozygous for the G170R mutation, pyridoxine is an enzyme co-factor and decreases urine oxalate ex...

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Udgivet i:Am J Kidney Dis
Main Authors: Lorenz, Elizabeth C., Lieske, John C., Seide, Barbara M., Olson, Julie B., Mehta, Ramila, Milliner, Dawn S.
Format: Artigo
Sprog:Inglês
Udgivet: 2020
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7930154/
https://ncbi.nlm.nih.gov/pubmed/32891627
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.ajkd.2020.07.017
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