Medical Term For Congenital Abnormality Of The Hindfoot
One of the most common inherited disorders affecting connective tissue Marfan syndrome MFS is an autosomal dominant condition with a reported incidence of 1 in 3000 to 5000 individuals12 The defect is in the FBN1 gene of chromosome 15 which produces fibrillin a connective tissue protein34 There is a broad range of clinical severity associated with. We consider any soft tissue injury or abnormality involving the soft tissues of the body whether congenital or acquired when an acceptable medical sources documents the need for ongoing surgical procedures and associated medical treatments to restore function of the affected body parts see 10100P1.
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