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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.
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.
Area of Science:
- Nephrology
- Genetics
- Pathology
Background:
- Alport syndrome (AS) is a rare, progressive hereditary kidney disease.
- It is characterized by sensorineural hearing loss, visual abnormalities, and kidney dysfunction.
- AS results from mutations in the collagen type IV alpha-4 (COL4A4) gene.
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