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In many cases, the patient may have few or very minor outward signs of the disorder, and the diagnosis may be missed until the patient develops vision problems or cardiac symptoms.
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Which president had Marfan's Syndrome?
Abraham Lincoln was thought to have Marfan syndrome. This has not been proven however, and many researchers think he may have had a different disorder instead.
If joe has the marfan syndrome and has a child some day what are the probaliblities that his chaild will have marfan?
There is a 100% probability of his child having Marfan's syndrome. The syndrome is carried by the FBN1 gene, and is dominant so there is no way to avoid having the disease. However the severity of it may vary from mild to severe, so his child may suffer from a mild form of the syndrome.
Why are eye conditions important in diagnosing cases of Marfan syndrome?
Although the visual problems that are related to Marfan syndrome are rarely life-threatening, they are important in that they may be the patient's first indication of the disorder.
How can the chest of Marfan syndrome be deformed?
A few patients with Marfan may have a pectus excavatum on one side of their chest and a pectus carinatum on the other.
Is marfan syndrome a genetic disease?
Yes, Marfan syndrome is a genetic disorder. It is not a disease. It is caused by a mutation in fibrillin and is an autosomal dominant mutation. This means that if you have a Marfan causing mutation, you have Marfan, and you have a 50/50 chance of passing it on to any children you may have. Severity of Marfan can vary within a family, even though all affected family members have the same mutation. It can not skip generations.
Kyphosis may develop in what areas of the spine in those suffering from Marfan syndrome?
Marfan patients may develop kyphosis either in the upper (thoracic) spine or the lower (lumbar) spine.
How does a person inherit marfan syndrome?
Marfan syndrome is an inherited disorder that is typically passed down from one generation to the next through an autosomal dominant pattern of inheritance. This means that if one parent carries the Marfan syndrome gene, there is a 50% chance that they will pass it on to each of their children. In some cases, Marfan syndrome may also occur as a result of a spontaneous genetic mutation.
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.
Children with Marfan syndrome may benefit from what counseling?
Children and adolescents with Marfan may benefit from supportive counseling regarding appearance, particularly if their symptoms are severe and causing them to withdraw from social activities.
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 is everyday life like for people with marfan syndrome?
Everyday life for someone who has Marfan syndrome is not too bad. They may be self conscious about how they look and have trouble learning new things but they can function as a normal human being in everyday life.
The face and spine of a Marfan syndrome may have what appearance?
The patient's face may also be long and narrow, and he or she may have a noticeable curvature of the spine.
