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Article

Genetic testing and glomerular hematuria-A nephrologist's perspective.

American journal of medical genetics. Part C, Seminars in medical genetics - 1 Sept 2022

Kashtan Clifford E

Abstract excerpt

Alport syndrome is an inherited disorder of the kidneys that results from variants in three collagen IV genes-COL4A3, COL4A4, and COL4A5. Early diagnosis and pharmacologic intervention can delay the progression of chronic kidney disease and the onset of kidney failure in patients with Alport syndrome. This article describes the evolution of approaches to the diagnosis and early treatment of Alport syndrome.

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Share to Nephritis, Hereditary
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 35775584
DOI: 10.1002/ajmg.c.31987
PMCID: PMC9796064

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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