Essay on Marfan Syndrome




Marfan syndrome MFS is a rare, autosomal dominant, multisystem disorder manifesting with skeletal, ocular, cutaneous, and cardiovascular symptoms. Significant clinical overlap with other systemic Marfans syndrome: a case report and pictorial essay. Quote this: Marfan syndrome is a systemic disorder of connective tissue caused by mutations in the extracellular matrix protein. Marfan syndrome is a genetic condition. Symptoms can affect people with a change in the FBN, which plays a role in connective tissue formation. Not everyone with this change will develop. One of the most common hereditary disorders affecting connective tissue, Marfan syndrome MFS, is an autosomal dominant disorder with a reported incidence in individuals. 1 2 The defect is in the FBN, which produces fibrillin, a connective tissue protein. 3 4 There is a wide range of clinical,





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