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Doctor insights on: Marfan Life

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Do bones close normally for Marfans pts or do they remain open longer even causing added growth in 30somethings? Can Marfans develop late in life (30s)

Do bones close normally for Marfans pts or do they remain open longer even causing added growth in 30somethings? Can Marfans develop late in life (30s)

Marfans: Rapid growth of bones in childhood, the epiphyses should fuse at the usual time. Marfans may be identified later in life, but it is a genetic disorder that is present at birth. ...Read more

Dr. Scott McLean
335 Doctors shared insights

Marfan Syndrome (Definition)

An inherited connective tissue disorder where body shape is long thin arms hands and fingers and arm length ...Read more


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Is marfan's syndrome asociated with a shortened life span?

Is marfan's syndrome asociated with a shortened life span?

Yes: Marfan's syndrome patients die from complications of aortic valve widening. If this is treated with inderal, (propranolol) progression is slower and patients live longer. In addition, if heart valve surgey is performed electivelly patients live longer. Untrated patients have a life span of 32 years. ...Read more

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I have Marfan syndrome. Is there tests that can prolong my life expectancy?

I have Marfan syndrome. Is there tests that can prolong my life expectancy?

An echocardiogram: If you have marfan syndrome, you should be aware that your cardiologist can use ultrasound to watch for the gradual enlargement of your aorta. Depending on your age, height, and weight, she can determine whether your aorta is growing larger than normal and recommend either medicine, like a beta blocker, or surgery to prevent dissection or rupture of the aorta. ...Read more

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Is Marfans discovered @ an early age w/ symptoms seen early or can abnormal tallness come about later in life like almost 2 decades after puberty ends?

Is Marfans discovered @ an early age w/ symptoms seen early or can abnormal tallness come about later in life like almost 2 decades after puberty ends?

May be later: You are born with the condition but manifestations may vary. Diagnosis may not be made till adulthood or not until a serious complication occurs. See this review:http://www. Uptodate. Com/contents/marfan-syndrome-the-basics? Source=search_result&search=marfan+syndrome&selectedTitle=1%7E105 ...Read more

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What is the average life span of someone who has eds or marfans?

What is the average life span of someone who has eds or marfans?

Generally, normal: People with eds generally have a normal lifespan. Though, those with the rare vascular type of eds have a high risk of sudden death from organ or vessel rupture. Heart-related complications can shorten the lifespan of people with marfan syndrome, though many live into their 60's and 70's (i.e. Normal lifespan) with careful medical management. ...Read more

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For someone with Marfan syndrome. Is there treatments that can prolong his life expectancy?

For someone with Marfan syndrome. Is there treatments that can prolong his life expectancy?

Several treatments!: Yes! children and adults with marfan syndrome can have gradual widening of the aorta - the major artery connected to your heart. Sometimes the aorta becomes so weak that it breaks. But your cardiologist can use an ultrasound machine to watch your aorta very carefully. She can treat you with medicines to slow down the enlargement, and your chest surgeon can even replace your aorta if necessary. ...Read more

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Can you tell me why there are often life-threatening aortic defects associated with marfan's syndrome?

Can you tell me why there are often life-threatening aortic defects associated with marfan's syndrome?

Firbrillin 1: In short, problem in Marfan's is a misfolding of a protein involved in the structure of connective tissue in various parts of the human body, notably in tissues such as mitral and aortic valves and aorta, which can lead to mitral valve prolapse, aortic dilation and aneurysms, aortic regurgitation, aortic dissection, etc along with extra cardiac manifestations. ...Read more

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I heard that abraham lincoln had marfans. Is that why he was so tall and thin?

I heard that abraham lincoln had marfans. Is that why he was so tall and thin?

Controversial: A very controversial subject, but unconfirmed. Individuals with marfan's syndrome have armspans greater than height, which represents the primary diagnostic criteria. ...Read more

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What is Marfan syndrome?

Genetic disorder: Of connective tissue that affects many bodily systems. The national marfan foundation has a very nice website that will answer any questions you have about marfan syndrome. Go to www. Marfan. Org. ...Read more

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What is Marfan syndrome?

Marfans/ehler danlos: Marfan syndrome is a connective tissue disorder, tissues that strengthen bodies structures. In most cases it is inherited condition, but approx 30% of patients have no family history tall arms and height, affects lungs, heart and aorta, eyes causing cataract, skin problems, and tissue covering the spinal chord. ...Read more

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What causes Marfan syndrome?

What causes Marfan syndrome?

Genetic mutation: Marfan syndrome is caused by a gene mutation (in the fbn1 gene). A mutation leads to defective, weakened connective tissue throughout the body. Symptoms show up in the parts of the body where shape and structural integrity relies a lot on the weakened type of connective tissue. ...Read more

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What exactly is Marfan syndrome?

What exactly is Marfan syndrome?

Genetic disorder: Fbn1 gene controls connective tissue metabolism. If there are mutations or repeats, then marfa's will result. The symptoms are the result of malformed collagen. So dislocated lens in eye, heart valve problems, scoliosis, pneumothorax, artery problems may occur. Most cases are inherited, but occasionally marfan's occurs from a spontaneous mutation. This gene can be tested for in a blood specimen. ...Read more

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How dangerous is Marfan syndrome?

How dangerous is Marfan syndrome?

Marfan syndrome: Affects the body's connective tissue and can cause problems in the eyes, joints, and heart. Marfan syndrome has no cure, but doctors can provide symptomatic management. ...Read more

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Common symptoms of Marfan's syndrome?

Marfan Syndrome: There is significant variability in how marfan syndrome presents in people. Possibly symptoms include: tall height; long arms, legs, fingers & toes, heart murmur, curved spine, flat feet, nearsightedness & deformity of the breast bone. ...Read more

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How to know if I have Marfan syndrome?

Marfan syndrome: Affects the body's connective tissue and can cause problems in the eyes, joints, and heart. Marfan syndrome has no cure, but doctors can provide symptomatic management. ...Read more

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How to tell if I have Marfan syndrome?

See the details: If you are tall, have very flexible joints, have any issues with the lenses of your eyes as well as other numerous finding on exam, you may have it. Have your doctor take a look or refer you to a rheumatologist. ...Read more

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I might have marfan, what should I do?

Med Eval: See your doctor. He or she can determine if you meet the international criteria for diagnosis. ...Read more