A case of concurrent Alport syndrome and Nail-patella syndrome posing diagnostic challenge without genetic testing

Hereditary glomerular basement membrane disease is a group of conditions caused by genetic mutations in the development and maintenance of the glomerular basement membrane. Alport syndrome is a classic example caused by variants in the genes COL4A3, COL4A4, or COL4A5. Less common example includes nail-patella syndrome (LMX1B-associated nephropathy), which is caused by variants in the LMX1B gene. The manifestations of LMX1B-associated nephropathy and Alport syndrome can overlap because they share abnormalities in type IV collagen, and this can sometimes cause diagnostic challenges. We describe a case of focal segmental glomerulosclerosis with the genetic test revealing concurrent variants of both Alport syndrome and nail-patella syndrome after noting features of nail-patella syndrome on clinical examination, although the kidney biopsy showed features compatible with Alport syndrome. Our case highlighted the importance of astute clinical examination backed up by genetic testing, which aids in diagnosis and subsequent management.

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Publication Details

Journal
BMC Nephrology
Published
2025-11-26
DOI
https://doi.org/10.1186/s12882-025-04606-1
Primary Topic
Cell Adhesion Molecules Research
Type
article
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article

A case of concurrent Alport syndrome and Nail-patella syndrome posing diagnostic challenge without genetic testing

Kai-Ming Chow, Michelle S. Yau, Cheuk‐Chun Szeto, Winston Wing‐Shing Fung et al.
BMC Nephrology
Cell Adhesion Molecules Research
article

A case of concurrent Alport syndrome and Nail-patella syndrome posing diagnostic challenge without genetic testing

Kai-Ming Chow, Michelle S. Yau, Cheuk‐Chun Szeto, Winston Wing‐Shing Fung, Shuk-ching Josephine Chong, Pensi Ping Hei Lam
article en

Abstract

Hereditary glomerular basement membrane disease is a group of conditions caused by genetic mutations in the development and maintenance of the glomerular basement membrane. Alport syndrome is a classic example caused by variants in the genes COL4A3, COL4A4, or COL4A5. Less common example includes nail-patella syndrome (LMX1B-associated nephropathy), which is caused by variants in the LMX1B gene. The manifestations of LMX1B-associated nephropathy and Alport syndrome can overlap because they share abnormalities in type IV collagen, and this can sometimes cause diagnostic challenges. We describe a case of focal segmental glomerulosclerosis with the genetic test revealing concurrent variants of both Alport syndrome and nail-patella syndrome after noting features of nail-patella syndrome on clinical examination, although the kidney biopsy showed features compatible with Alport syndrome. Our case highlighted the importance of astute clinical examination backed up by genetic testing, which aids in diagnosis and subsequent management.

BMC NephrologyVol. 26(1)
Chinese University of Hong Kong (HK), Prince of Wales Hospital (CN)
Openalex Percentile: Top 53%
Cell Adhesion Molecules Research
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