Marfan syndrome (MFS) is an autosomal dominant disorder of the body’s connective tissue, caused by mutations in the fibrillin-1 ( FBN1 ) gene. The estimated prevalence of the syndrome is… Click to show full abstract
Marfan syndrome (MFS) is an autosomal dominant disorder of the body’s connective tissue, caused by mutations in the fibrillin-1 ( FBN1 ) gene. The estimated prevalence of the syndrome is 1 in 5,000 (1).
               
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