[Genetic aspects of primary hyperoxaluria: diagnostics and treatment].

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ID: 68594
2019
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Abstract
Primary hyperoxaluria is a group of inherited metabolic diseases characterized by increased formation of calcium-oxalate stones in kidneys with development of nephrolithiasis and chronic kidney disease. The article summarizes the modern information on the diagnostics and treatment of the disorder depending on genotype of the patient (AGXT, GRHPR, HOGA1 genes). The evaluation of the molecular genetic aetiology of the kidney stone disease contributes to the personalized treatment and prevention of the pathology in the patients and their relatives.
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filippova2019geneticurologiia Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Filippova, T V;Svetlichnaya, D V;Rudenko, V I;Alyaev, Y G;Shumikhina, M V;Azova, M M;Subbotina, T I;Gadzhieva, Z K;Asanov, A Yu;Litvinova, M M;
Journal urologiia (moscow, russia : 1999)
Year 2019
DOI DOI not found
URL URL not found
Keywords
treatment urolithiasis agxt grhpr hoga1 kidney stone disease oxalosis primary hyperoxaluria

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