Alport Syndrome With a Rare Collagen Type IV Alpha-4 (COL4A4) Gene Mutation: A Case Report

Akshaya Rana1, Surekha Tayade1

  • 1Department of Obstetrics and Gynaecology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

Cureus
|October 14, 2024
PubMed
Summary

Alport syndrome (AS), a hereditary kidney disease caused by COL4A4 gene mutations, presents unique renal and extrarenal findings. This case highlights a 15-year-old boy with AS, showing characteristic symptoms and microscopic findings.

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