Marfan syndrome is the most common connective tissue disorder, with an incidence of 1 in 10,000. Marfan syndrome is autosomal dominantly inherited and associated with FBN-1 gene mutations. The alteration in the microfibril protein structure results in ocular, skeletal, and cardiovascular abnormalities, such as mitral valve prolapse and aortic root dilatation. Presented is an image of a 35 years old man with Marfan syndrome and a pectus excavatum (funnel chest).
2011 x 2500 pixels
Print Size @ 300 dpi
7 x 8 inches / 17 x 21 cm
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