Article

Severe Hyperferritinemia with Preserved Transferrin Saturation in Genetically Confirmed X-Linked Alport Syndrome: A Case Report

2026-03-27

Abstract excerpt

<title>Abstract</title> Background Alport syndrome is an X-linked inherited kidney disease caused by mutations in type IV collagen genes (COL4A3, COL4A4, and COL4A5) that affect the glomerular basement membrane and can lead to sensorineural hearing loss and eye abnormalities. This disease, which can cause hematuria, proteinuria, and in more severe cases chronic kidney disease, is characterized by bilateral an...

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Literature Corpus work: bb47f4e2-f769-59aa-9c69-3d2cf0cb0272
DOI: 10.21203/rs.3.rs-8970844/v1

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