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Article

Familial hematuria due to type IV collagen mutations: Alport syndrome and thin basement membrane nephropathy.

Current opinion in pediatrics - 1 Apr 2004

Kashtan Clifford E

Abstract excerpt

PURPOSE OF REVIEW: Recent molecular genetic studies have shown that mutations in type IV collagen account for a significant proportion of patients with persistent glomerular hematuria. This review will discuss the implications of these findings for the diagnosis and management of persistent glomerular hematuria. RECENT FINDINGS: Type IV collagen mutations are associated with a continuum of disease severity....

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 15021198
DOI: 10.1097/00008480-200404000-00011

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Familial hematuria due to type IV collagen mutations: Alport syndrome and thin basement membrane nephropathy.PMID 15021198Read ↗

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