DelveInsight Evaluation of Marfan Syndrome Market Landscape
Marfan syndrome is an autosomal dominant connective tissue disorder caused by mutations in the FBN1 gene, which encodes the glycoprotein fibrillin-1. This structural protein is a vital component of the extracellular matrix, providing the necessary elasticity and support for various tissues throughout the human body. When fibrillin-1 production is compromised, it leads to a cascade…
