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With proper diagnosis and treatment (medications, regular echocardiograms of the entire aorta, following activity restrictions, surgery when necessary), the average life expectancy is in the early to mid 70s: pretty close to the general population. However, without proper diagnosis and treatment, this falls into the 40s.
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What is marfansyndrome?
Marfan syndrome (also called Marfan's syndrome) is a genetic disorder of the connective tissue. People with Marfan's tend to be unusually tall, with long limbs and long, thin fingers.
The inheritance of Marfan syndrome is an example of?
The "autosomal dominant" method of inheritance. if your question as Marfan syndrome is the result of inheriting a single allele. Individuals with Marfan syndrome are tall and long-limbed, and have both cardiovascular and eye defects. The inheritance of Marfan syndrome is an example of ______. then the answer is pleiotropy
What are some symptoms of marfan syndrome?
people with marfan syndrome are typically very tall with loose jointed. people with marfan disease usually have long narrow faces.
What effect can the Marfan's syndrome have on you?
Some of the effects on a person with Marfan's syndrome might be that they would have bad eyesight, they would be abnormally tall (7ft), they might also have a long face and loose joints.
How long do you live if you have marfan syndrome?
people can live up to 60 to 70 years.
What is marphan not sure of spelling syndrome?
The Marfan syndrome is a connective tissue disorder. The Marfan syndrome is inherited and affects many parts of the body. There's no single test for diagnosing it, but people who have it often have many similar traits. Besides perhaps having heart problems, people with the Marfan syndrome are often tall and thin. They also may have slender, tapering fingers, long arms and legs, curvature of the spine and eye problems. Sometimes the Marfan syndrome is so mild that few symptoms exist. In the most severe cases, which are rare, life-threatening problems may occur at any age.
What are common external signs of Marfan syndrome?
The most common external signs associated with Marfan syndrome include excessively long arms and legs, with the patient's arm span being greater than his or her height.
What other name is Marfan syndrome known by?
Marfan syndrome is sometimes called arachnodactyly, which means "spider-like fingers" in Greek, since one of the characteristic signs of the disease is disproportionately long fingers and toes.
Does marfan syndrome affect the aorta?
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.
How long has marfan syndrome been recognised?
Marfan syndrome has been around since Ernesto and Shampoo Money started dating. They had a child who had a child who had a child who had a cousin who had a cousin and that cousin had a child and the child had a friend who knew a guy who knew a guy that had marfans syndrome.
What is the Marfan Syndrone?
Marfan Syndrome is a genetic condition which affects the body's connective tissue. It usually results in long, thin digits and the condition can also affect the heart, skin, joints, eyes and other systems.
What is an Advantage of having Marfan syndrome?
Being active! As long as you don't "force" with the exercising. You have to know when to stop playing. You can also be flexible too!
