Article

Possible break-down of redox homeostasis in Beals-Hecht syndrome

2025-04-21

Abstract excerpt

<title>Abstract</title> <p>Beals-Hecht (BH) syndrome is a rare autosomal dominant disorder caused by a mutation of the <italic>FBN-2</italic> gene that codifies for fibrillin-2 (FBN-2) and its nosology includes congenital contractural arachnodactyly. The aim of this study was to evaluate the possible breakdown of redox homeostasis in the thoracic aortic aneurysm (TAA) in BH. We determinate OS markers such as malo...

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Literature Corpus work: 8771182f-cdc1-5e81-abd7-73d69de6408b
DOI: 10.21203/rs.3.rs-6306791/v1

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