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Marfan syndrome is a genetic disorder that affects the body’s connective tissue, which is the tissue that holds all the organs and tissues together. People with Marfan syndrome often have a tall, thin build, long arms, legs, fingers, and toes, and flexible joints. They may also have distinct facial features like a long face, deep-set eyes, and a small chin. Scoliosis is a condition where the spine curves to the side, making it look like an “S” or “C” shape. This can cause uneven shoulders and hi
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JuMed on Instagram: "Marfan Syndrome — more than just “being tall.” Marfan is a connective-tissue disorder caused by a mutation in the FBN1 (Fibrillin-1) gene. When fibrillin is faulty, the elastic fibers in your body weaken — and the effects hit multiple systems: 🦴 Skeletal: tall, long limbs, long fingers (arachnodactyly), chest wall deformities 👁️ Eyes: lens dislocation, early myopia ❤️ Heart & Aorta: aortic root dilation, aneurysm risk, mitral valve prolapse — the most serious complications
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