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What Does Marfan Syndrome Look Like? 37 photos · 1,377,634 views. By: National Marfan Foundation. Explore this photo album by National Marfan Foundation on Flickr!
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Harder-to-detect signs of Marfan syndrome include heart problems, especially those related to the aorta, the large blood vessel that carries blood away from the heart to the rest of the body. Other signs can include sudden lung collapse and eye problems, including severe nearsightedness, dislocated lens, detached retina, early glaucoma, and ...
- What Is Marfan Syndrome?
- What Medical Problems Are Associated with Marfan Syndrome?
- What Are The Risk Factors of Marfan Syndrome?
- How Is Marfan Syndrome Diagnosed?
Marfan syndrome is a rare genetic disorder of the connective tissue, affecting the skeleton, lungs, eyes, heart and blood vessels. The condition is caused by a defect in the gene that tells the body how to make fibrillin-1, often from a parent who is also affected. One quarter of cases may be the result of a spontaneous gene mutation. Fibrillin-1 i...
Marfan syndrome primarily affects the cardiovascular and skeletal systems. People with the condition may also have vision problems; many are near-sighted, and about 50 percent suffer from dislocation of the ocular lens. Marfan syndrome affects the cardiovascular system by making the aorta (an artery that begins at the heart and is the largest in th...
The only known risk factor is having a parent with Marfan syndrome, as this is a condition that is most often inherited. A person with Marfan syndrome has a 50 percent chance of passing along this condition to each child. However, one out of every four people with Marfan syndrome also acquire the condition due to a spontaneous genetic mutation.
People with Marfan syndrome exhibit different combinations of symptoms. Because symptoms of the condition overlap with other related connective tissue disorders, it is vitally important that your physicians be knowledgeable about Marfan syndrome. Tests include: 1. Echocardiogram— a sound wave picture of the heart and aorta — by a cardiologist 2. Sl...
Mar 22, 2024 · Marfan syndrome is an inherited disorder that affects connective tissue — the fibers that support and anchor your organs and other structures in your body. Marfan syndrome most commonly affects the heart, eyes, blood vessels and skeleton.
People with Marfan syndrome have feet that are long and slender. Extra-long bones and extra-loose ligaments can make the feet weak and less able to manage the pressure when people stand up. Some features that are common in Marfan syndrome are: Long, thin feet. Flat feet (very low arch) or extra-high arch.
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Children with Marfan syndrome may display just a few symptoms, or many. The symptoms may be mild or severe. It is a combination of various characteristics — including issues with the heart, eyes, and musculoskeletal system — that may alert your child's doctor to the possibility of Marfan syndrome.
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Dec 6, 2023 · Seek immediate emergency medical attention for symptoms like sudden severe pain in your chest, back, or belly; shortness of breath; or stroke-like symptoms, such as sudden muscle weakness. These might be caused by an aortic dissection or rupture. Sometimes the heart valves are affected in Marfan syndrome.
