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Marfan syndrome is an autosomal-dominant genetic disorder caused by a mutation in the FBN1 gene, affecting the skeletal, ocular, and cardiovascular systems. Characterized by aortic root dilation, lens dislocation, and unique body structure. Early diagnosis is crucial to prevent aortic dissection
#lens dislocation#fbn1 gene#myopia#hypermobile joints#mitral valve prolapse
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