Autosomal Dominant Alport Syndrome Diagnosed in an Elderly Man

Autosomal dominant Alport syndrome (ADAS) is an uncommon diagnosis and is often missed in patients with chronic kidney disease of unknown origin unless specific genetic testing is performed. It results from heterozygous mutations in the COL4A3 and COL4A4 genes. The clinical presentation is variable but generally milder than that of X-linked or autosomal recessive Alport syndrome. In this article, we present the case of a 78-year-old man who was diagnosed with ADAS during evaluation in a nephrology clinic. We also discuss the condition and the challenges related to the terminology surrounding Alport syndrome.

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Journal
Cureus
Published
2025-10-16
DOI
https://doi.org/10.7759/cureus.94725
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Autosomal Dominant Alport Syndrome Diagnosed in an Elderly Man

Farid Arman, Mrinalini Sarkar, Reza Khorsan
Cureus
Cell Adhesion Molecules Research
article

Autosomal Dominant Alport Syndrome Diagnosed in an Elderly Man

Farid Arman, Mrinalini Sarkar, Reza Khorsan
article en

Abstract

Autosomal dominant Alport syndrome (ADAS) is an uncommon diagnosis and is often missed in patients with chronic kidney disease of unknown origin unless specific genetic testing is performed. It results from heterozygous mutations in the COL4A3 and COL4A4 genes. The clinical presentation is variable but generally milder than that of X-linked or autosomal recessive Alport syndrome. In this article, we present the case of a 78-year-old man who was diagnosed with ADAS during evaluation in a nephrology clinic. We also discuss the condition and the challenges related to the terminology surrounding Alport syndrome.

CureusVol. 17(10)
University of California, Los Angeles (US)
Openalex Percentile: Top 62%
Cell Adhesion Molecules Research
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