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What is the most serious complication from Marfan syndrome?
Aortic enlargement. This is the most serious potential complication of Marfan syndrome.
What are other names for Marfan Syndrome?
Marfan Syndrome is also known as Marfan's disease and hereditary connective tissue disorder. In some contexts, it may be referred to as Marfan syndrome type I or simply as a connective tissue disorder. However, the most common and widely recognized name remains Marfan Syndrome.
How common is marfan syndrome?
Marfan's syndrome is the most common genetic disorder of connective tissue. It occurs in about every 10,000 to 20,000 individuals.
What portion of Marfan syndrome patients develop myopia?
Myopia (nearsightedness). Most patients with Marfan develop nearsightedness, usually in childhood.
What part of the heart is most likely to develop infection in Marfan syndrome sufferers?
In patients with Marfan, it is the abnormal mitral valve that is most likely to become infected.
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.
Why is a diagnosis of Marfan syndrome easier to make in adults than in children?
Most of the external features of Marfan syndrome become more pronounced as the patient gets older, so that diagnosis of the disorder is often easier in adults than in children.
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.
Is marfan's syndrome fatal?
Marfan syndrome is not inherently fatal, but it can lead to serious complications that may shorten lifespan if not properly managed. The most significant risks involve cardiovascular issues, particularly aortic dilation and dissection, which can be life-threatening. With early diagnosis and appropriate medical care, many individuals with Marfan syndrome can lead relatively normal lives. Regular monitoring and treatment can help mitigate the risks associated with the condition.
What medical disease did Abraham lincon have?
Theres been an ongoing debate on this issue. Most 'experts' believe he suffered from Marfans disease; he also is claimed to have had smallpox. Some believe he also had cancer. I doubt we will ever really know the truth.
Marfan syndrome may be given what commonly used beta-blockers?
The most commonly used beta-blockers in Marfan patients are propranolol (Inderal) and atenolol (Tenormin). Patients who are allergic to beta-blockers may be given a calcium blocker such as verapamil.
Can marfans syndrome kill me?
Yes, Marfan syndrome can lead to life-threatening complications, particularly involving the cardiovascular system. The most serious risk is aortic dissection or rupture, which can occur when the aorta becomes weakened and dilated. Regular monitoring and management by healthcare professionals can help mitigate these risks and improve life expectancy for those with the condition. If you have concerns about Marfan syndrome, it's essential to discuss them with a medical professional.
