Literature DB >> 35896809

Familial acute aortic dissection associated with a novel ACTA2 germline variant.

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.
© 2022. The Author(s).

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


  2 in total

1.  Inflammatory thoracic aortic aneurysm (lymphoplasmacytic thoracic aortitis): a 13-year-experience at a German Heart Center with emphasis on possible role of IgG4.

Authors:  Abbas Agaimy; Michael Weyand; Thomas Strecker
Journal:  Int J Clin Exp Pathol       Date:  2013-08-15

Review 2.  α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies.

Authors:  Shi-Min Yuan
Journal:  Braz J Cardiovasc Surg       Date:  2015 Nov-Dec
  2 in total

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