Marfan syndrome
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British pronunciation/mˈɑːfən sˈɪndɹəʊm/
American pronunciation/mˈɑːɹfən sˈɪndɹoʊm/

"Marfan syndrome"Meghatározása és Jelentése

Marfan syndrome
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Marfan-szindróma

a genetic disorder characterized by connective tissue abnormalities, leading to various physical manifestations including tall stature, long limbs, joint hypermobility, and cardiovascular issues
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What is "Marfan syndrome"?

Marfan syndrome is a genetic disorder that affects the body's connective tissue, which provides support and structure to various tissues and organs. It is caused by changes in the gene that instructs the body to make fibrillin, a protein that helps give connective tissue its strength and flexibility. Marfan syndrome can affect many parts of the body, including the heart, blood vessels, bones, joints, and eyes. People with Marfan syndrome may be tall and thin with disproportionately long arms, legs, fingers, and toes. They may also have chest deformities, scoliosis, and a higher risk of developing heart problems. Treatment typically focuses on managing symptoms and preventing complications through regular monitoring and medical actions such as medications, surgery, or other specialized treatments.

Marfan syndrome

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