An atypical case of Marfan syndrome

Abstract

Marfan syndrome is a relatively rare disease characterized by a primary congenital defect of connective tissue, which is based on dystrophic changes in fibrous structures caused by impaired metabolism of chondroitinseric and glucuronic acid. The classic signs of this syndrome are lesions of the musculoskeletal system, eyes, heart and large vessels.

Full Text

##article.viewOnOriginalSite##