Marfan Syndrome Pipeline Therapies and Market Forecast Overview
Marfan syndrome is a genetic disorder impacting connective tissue, arising from mutations in the fibrillin-1 gene (FBN1). This hereditary condition affects numerous body systems—primarily the eyes, skeletal structure, and cardiovascular network. Because it follows an autosomal dominant inheritance pattern, each child of an affected individual has approximately a 50% chance of inheriting the condition. Despite…
