A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections

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 associatio...

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Autores principales: Takeda, Miki, Minagawa, Tadanori, Hiranuma, Wakiko, Matsuoka, Takayuki, Shimizu, Takuya, Kawamoto, Shunsuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese College of Angiology / The Japanese Society for Vascular Surgery / Japanese Society of Phlebology 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257394/
https://www.ncbi.nlm.nih.gov/pubmed/35860818
http://dx.doi.org/10.3400/avd.cr.22-00010
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author Takeda, Miki
Minagawa, Tadanori
Hiranuma, Wakiko
Matsuoka, Takayuki
Shimizu, Takuya
Kawamoto, Shunsuke
author_facet Takeda, Miki
Minagawa, Tadanori
Hiranuma, Wakiko
Matsuoka, Takayuki
Shimizu, Takuya
Kawamoto, Shunsuke
author_sort Takeda, Miki
collection PubMed
description 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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spelling pubmed-92573942022-07-19 A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections Takeda, Miki Minagawa, Tadanori Hiranuma, Wakiko Matsuoka, Takayuki Shimizu, Takuya Kawamoto, Shunsuke Ann Vasc Dis Case Report 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. Japanese College of Angiology / The Japanese Society for Vascular Surgery / Japanese Society of Phlebology 2022-06-25 /pmc/articles/PMC9257394/ /pubmed/35860818 http://dx.doi.org/10.3400/avd.cr.22-00010 Text en © 2022 The Editorial Committee of Annals of Vascular Diseases. https://creativecommons.org/licenses/by/2.5/This article is distributed under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided the credit of the original work, a link to the license, and indication of any change are properly given, and the original work is not used for commercial purposes. Remixed or transformed contributions must be distributed under the same license as the original.
spellingShingle Case Report
Takeda, Miki
Minagawa, Tadanori
Hiranuma, Wakiko
Matsuoka, Takayuki
Shimizu, Takuya
Kawamoto, Shunsuke
A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
title A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
title_full A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
title_fullStr A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
title_full_unstemmed A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
title_short A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
title_sort case of alport syndrome associated with recurrent stanford type b aortic dissections
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257394/
https://www.ncbi.nlm.nih.gov/pubmed/35860818
http://dx.doi.org/10.3400/avd.cr.22-00010
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