Article
Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.
Nephrologie & therapeutique - 1 May 2017
Soliman Neveen A, Nabhan Marwa M, Abdelrahman Safaa M, Abdelaziz Hanan, Helmy Rasha, Ghanim Khaled, Bazaraa Hafez M, Badr Ahmed M, Tolba Omar A, Kotb Magd A, Eweeda Khaled M, Fayez Alaa
Abstract excerpt
BACKGROUND AND AIM: Primary hyperoxalurias are rare inborn errors of metabolism resulting in increased endogenous production of oxalate that leads to excessive urinary oxalate excretion. Diagnosis of primary hyperoxaluria type 1 (PH1) is a challenging issue and depends on diverse diagnostic tools including biochemical analysis of urine, stone analysis, renal biopsy, genetic studies and in some cases liver biopsy...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.