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Article

Three-stage extensive aortic substitution in a young man with a variant of uncertain significance in myosin heavy chain 11 gene.

Vascular - 1 Jun 2026

Pascucci Federico, Donati Tommaso, Vallabini Albino, Cassese Mauro, Tshomba Yamume

Abstract excerpt

BackgroundNon-syndromic hereditary aortic diseases are caused by mutations in genes encoding for connective tissue components, involving structural integrity of aortic tissue. Amongst them, MYH11 gene mutation is a known causative factor for aortic diseases, especially in young patients.Research DesignWe report the case of a 37 years-old male which came to our attention for an acute DeBakey type I aortic...

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Share to Aortic Aneurysm, Thoracic
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 40803037
DOI: 10.1177/17085381251359315
PMCID: PMC13195059

Genes

MYH11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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