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Does marfan syndrome affect the aorta?

Updated: 8/17/2019
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14y ago

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Yes. Marfan syndrome is a congenital disorder affecting the formation of fibrillin. In Marfan syndrome, the abnormal fibrillin is responsible for many of the findings of the disease. Hyperextensibility/hyperelasticity of joints is one of the hallmark signs. Pectus excavatum is another. People with Marfan syndrome are typically very tall and thin, with very long fingers and toes (arachnodactyly).

The fibrillin defect also affects the blood vessels, especially the large arteries, such as the aorta. Disordered fibrillin production causes these arteries to be weaker than normal, predisposing patients with Marfan syndrome to aortic dissections and rupture. This the major cause of death for patients with Marfan syndrome.

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Q: Does marfan syndrome affect the aorta?
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What impact does Marfan syndrome have on the ability to learn?

Marfan syndrome can affect learning abilities if a child experiences vision problems, attention deficits, or learning disabilities associated with the condition. However, with appropriate support and accommodations, individuals with Marfan syndrome can still achieve academic success. Regular monitoring and early intervention can help address any learning challenges that may arise.


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Marfan syndrome shows up at birth.


How does marfan syndrome affect your life?

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Does marfan syndrome affect life span?

Yes, Marfan syndrome does affect the life span of a human. It is shown that their life span is cut on average by one third.


How tall are people with marfan syndrome?

There is no set height for people with Marfan syndrome. There was even a man who had both dwarfism and Marfan syndrome! People with Marfan are USUALLY taller than unaffected family members, but not always. More important than a person's height are their ratios (arm span to height, upper torso to lower torso), flexibility, condition of their aorta, and condition of their eyes.


What is the IQ of a person suffering with marfan syndrome?

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Is marfan syndrome automsomal dominant?

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WHAT race does Marfan syndrome affect?

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What is the life expectincy of marfan syndrome?

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