Unusual combination of acute aortic dissection, Mayer-Rokitansky-Küster-Hauser syndrome, and 46,XX gonadal dysgenesis: A case report

Unusual combination of acute aortic dissection, Mayer-Rokitansky-Küster-Hauser syndrome, and 46,XX gonadal dysgenesis: A case report

BackgroundAcute Stanford type A aortic dissection (ATAAD) is a life-threatening disease. Elderly patients are the high-risk population for aortic dissection (AD). Young patients with AD usually have heritable connective tissue diseases such as Marfan syndrome and Loeys-Dietz syndrome. However, young...

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Bibliographic Details
Main Authors: Yifan Zeng, Yerong Hu, Bo Jiang, Ling Tan, Hao Tang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-11-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
aortic dissection
MRKH syndrome
46,XX gonadal dysgenesis
total aortic arch replacement
frozen elephant trunk
whole-exome sequencing
Online Access:https://www.frontiersin.org/articles/10.3389/fcvm.2022.1030160/full

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https://www.frontiersin.org/articles/10.3389/fcvm.2022.1030160/full

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