| Literature DB >> 35896809 |
Thomas Strecker1, Felix Wiesmueller2, Sabine Rudnik-Schöneborn3, Juliane Hoyer4, André Reis4, Michael Weyand5, Abbas Agaimy6.
Abstract
Aortic dissection is a life-threatening cardiovascular disease. Hereditary disorders are responsible for a small percentage of cases. Nonetheless, it is important to identify genetic causes, as they are often autosomal dominantly inherited and are of life-saving importance if we can identify persons at risk. Mutations of the ACTA2 gene are the most common cause of non-syndromic familial aortic disease. Exploration of the genetic background in suspected familial cases and determination of the exact etiology are mandatory for management and establishing appropriate follow-up strategies due to the risk of fatal recurrences. Herein, we present a 21-year-old male with a familial acute aortic dissection associated with novel ACTA2 germline variant and discuss the management and surveillance considerations.Entities:
Keywords: ACTA2 mutation; Aortic dissection; Cardiac surgery; Echocardiography, Computer tomography; Human genetics; Pathology
Year: 2022 PMID: 35896809 DOI: 10.1007/s00428-022-03366-9
Source DB: PubMed Journal: Virchows Arch ISSN: 0945-6317 Impact factor: 4.535