Ectopia Lentis with Retinal Detachment in a Patient with Marfan Syndrome: A Case Report
Marfan syndrome is an autosomal dominant hereditary connective tissue disease caused by mutations in the Fibrillin-1 gene located on chromosome 15q15-21.Fibrillin is a specific type of glycoprotein widely distributed throughout the body, contributing to the elasticity and load-bearing capacity of connective tissue.Marfan syndrome is a multisystem d