Marfan syndrome is an inherited disorder that affects connective tissue, which supports and anchors your organs and other structures in your body. Because connective tissue is such an integral part of your body,
Marfan syndrome may disrupt development and function in several sites. Most common are your heart, eyes, blood vessels and skeleton. They affect men, women, and children, and have been found among people of all races and ethnic backgrounds.
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| Marfan Syndrome |
The signs and symptoms of Marfan's degenerative disease develop progressively in the past few years. Some of the most common are long slender bones which make a man or woman exceedingly tall, long slender finger and toes, heart flaws and a incomplete dislocation of the lenses of the eyes. In extreme cases, the elastic fibers in the media of the aorta may well be damaged, leading to aneurysm.
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| Marfan Syndrome |
Marfan syndrome can also seriously affect the eyes and vision. The most serious signs and symptoms associated with
Marfan syndrome involve the cardiovascular system. The most serious complications of Marfan syndrome involve the heart and blood vessels.
Marfan syndrome can affect the aorta, the main blood vessel that supplies oxygen-rich blood to the body. It's very serious and can lead to severe heart problems or even death.
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| Marfan Syndrome |
There can be no specific test for
Marfan's syndrome as well as the analysis is made mostly on its symptoms. Treatment is aimed toward relieving warning signs and preventing health concerns. Some of the most common are surgery to repair aneurysm, eye defects as well as spinal curvature, and hormones therapy to stop the person from developing abnormally tall.
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| Marfan Syndrome |
The signs and symptoms mentioned might or might not show up together. The intensity can also} vary. In case you think that you are affected of this disorder, most especially if within your family relations historical past, you should instantly refer all of them a medical doctor.
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