Complete Atrioventricular Block in a Young Patient With Alport Syndrome: A Case Report
Complete atrioventricular block (AVB) has not been previously reported in patients with Alport syndrome with normal kidney function. We describe a rare case of a young man with Alport syndrome who developed complete AVB. Cardiac magnetic resonance imaging revealed no signs of inflammation or other abnormalities. Whole-exome sequencing identified several variants, but none alone could explain the heart block. We hypothesize that AVB may be a potential complication of Alport syndrome or the result of multiple variants. A permanent pacemaker was implanted, and a 6-month follow-up confirmed the irreversibility of the AVB.
Authors
- Yanjun Gong (ORCID: https://orcid.org/0000-0003-1281-1073)
- Qinhui Sheng
- Zuoyi Zhou (ORCID: https://orcid.org/0000-0002-8687-9196)
- Long Zhang (ORCID: https://orcid.org/0000-0002-7400-7737)
- Jianping Li
Institutions
- Peking University (CN)
- Peking University First Hospital (CN)
Publication Details
- Journal
- Annals of Internal Medicine Clinical Cases
- Published
- 2025-04-01
- DOI
- https://doi.org/10.7326/aimcc.2024.0412
- Primary Topic
- Cell Adhesion Molecules Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Peking University First Hospital
- Peking University
- National Key Research and Development Program of China