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How long do you live if you have marfan syndrome?
people can live up to 60 to 70 years.
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 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.
When marfan syndrome was discovered?
Marfan syndrome was first described by Antoine Marfan, a French pediatrician, in 1896. He identified the unique characteristics of the syndrome, including tall stature, long limbs, and heart problems.
The inheritance of Marfan syndrome is an example of?
The inheritance of Marfan syndrome is an example of an autosomal dominant genetic disorder. This means that a person only needs to inherit one copy of the mutated gene from a parent to develop the syndrome.
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 do people with turner syndrome live?
people (girls/women) with turner syndrome live as long as regular people do....turner syndrome does not affect life spancy
What gene is marfan syndrome?
Marfan syndrome is caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. These mutations can affect the structure and function of connective tissue, leading to the characteristic features of Marfan syndrome such as tall stature, long limbs, and heart abnormalities.
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 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.
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.
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.
