. . . Approximately 1 to 2 people out of 10,000 have Marfan syndrome. .

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This mutation results in an increase in a protein called transforming growth factor beta, or TGF-.

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. . Description. Marfan syndrome is a genetic condition that affects connective tissue, which plays a crucial role in forming skin, bones,. . . .

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Major symptoms include overgrowth of the long bones of the arms and legs, abnormal side-to.

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