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A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
Miki Takeda1, Tadanori Minagawa1, Wakiko Hiranuma1
1Department of Cardiovascular Surgery, Tohoku Medical and Pharmaceutical University, Sendai, Miyagi, Japan.
Abstract:
Alport syndrome is often characterized by renal dysfunction and hearing loss due to abnormalities in type IV collagen production. In this study, we report a rare case of recurrent aortic dissections that developed in a young patient with Alport syndrome over a short period. We discuss the associations between Alport syndrome and aortic dissection with a literature review and emphasize the need for regular follow-up of patients with Alport syndrome for early detection of aortic disease.
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