Doctor insights on:
Can People With Marfan Syndrome Live Long Lives
Varies by severity: People with mild marfan syndrome symptoms probably live a pretty normal lifespan. Those with severe symptoms can die from heart valve problems, rupture of the aorta, tension pneumothorax, etc..., before they reach old age. Of course, those with moderate symptoms will have a lifespan in between. ...Read moreSee 1 more doctor answer
Can you still have Marfan syndrome without haveing long limbs? I have all the other symptoms and my doctor thinks it's a possibility.
Unusual: Each patient with marfan syndrome has a different presentation. Without long limbs (arms/legs) it would be unusual to have true marfan syndrome, but those findings are not very important diagnostic criteria. The cardinal features aortic root dilation (aneurysm) and dislocated lenses. The website http://www.Marfan.Org is helpful to patients and physicians. ...Read moreSee 1 more doctor answer
I am a 17 year old female who is 6 feet 2 inches. I have very long fingers and toes an long, thin arms.Do I have Marfan syndrome? I am worried!
See cardiologis: Certain clinical features r required for the diag. Of marfan syndrome. Being thin, tall with long fingers, toes and extremities is not enough for the diagnosis but may be an indication for referral to a pediatric cardiologist, pediatric ophthalmologist and geneticist for a much broader evaluation to rule out other abnormalities in the heart, eye and skeletal system and skin consistent w marfan. ...Read moreSee 3 more doctor answers
Son has double joints, long limbs, long wrist, fingers & hands. Could it be Marfan syndrome? Something doesn't seem right.
Im f, 5'6(tall) , thin, long arms&legs, hands r big w/long fingers &are flexible, but my body is not flexible, narrow face&jaw, do I have Marfan syndrome?
Can be cryptic: Most people who are thin do not have a connective tissue disease (marfan syndrome.) there is a formal diagnostic approach for suspected marfan syndrome, though, and it is worth reading. Here is a link to a helpful site: http://www.Marfan.Org/expectations/diagnosis. ...Read moreSee 1 more doctor answer
Usually yes: A marfan syndrome person with a current or recent pneumothorax (collapsed lung) should not fly (unless the airplane stays close to his airport's altitude) because the decrease in outside air pressure as the airplane ascends can allow his pneumothorax to enlarge and compress the lungs and heart. ...Read moreSee 1 more doctor answer
Non-strenguous: Marfan syndrome persons should avoid contact sports. If symptoms are on the moderate to severe side, they can participate in non-contact, non-strenguous activities such as golf, bowling, walking, yoga, or tai-chi. If mild to moderate in severity, they can try non-contact, moderately strenguous activities such as biking or swimming. The national marfan foundation website is helpful. ...Read moreSee 1 more doctor answer
Rarely: Occasionally, a person with marfan syndrome will have normal height, but the majority of people with marfan syndrome tall. Even if people with marfan syndrome who have normal height, there long bones tend to be longer than typical, resulting in longer than typical arms, legs, and fingers. ...Read moreSee 1 more doctor answer
Do people with Marfan Syndrome ever stop growing in height and if so is it about the same time others without the disease stop growing ?
Yes : There are multiple potential. abnormalities associated with marfans, such as scoliosis, for example; but they do typically reach skeletal maturity (stop growing) at a similar age as those without marfans. In general, their height is taller than average and they tend to be slender. ...Read more
Visual disabilities: Marfan syndrome patients, if severe, can have disabilities involving vision, such as reading. Patients can have dislocated lens in the eyes (lens are out of position and cannot focus properly), retinal detachments (retina comes off the inside surface of the eyeballs), early cataracts (lens become cloudy), or early glaucoma (excess pressure inside the eyeballs). ...Read moreSee 1 more doctor answer
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
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 moreSee 1 more doctor answer
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 moreSee 1 more doctor answer
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