Question 1

what is marfan syndrome?

Accepted Answer

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.

Question 2

what causes marfan syndrome?

Accepted Answer

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.

Question 3

how dangerous is marfan syndrome?

Accepted Answer

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.

Question 4

how to know if i have marfan syndrome?

Accepted Answer

Connective tissue : Marfan is an inherited disorder of connective tissue. Which affects musculoskeletal system, blood vessels heart and eyes.
People with Marfan are thin and tall and have disproportionate long arms and legs, fingers and toes. An eye exam  to check for lens dislocation. Heart exam to check for dilatation of vessels and heart valves.
If  further study needed genetic tests are available.

Question 5

is marfan syndrome a sex-linked disease?

Accepted Answer

No: Marfan syndrome is an autosomal dominant connective tissue disorder caused by abnormal microfibrillin protein. If a parent is affected by the disorder, their offspring has a 50/50 chance of inheriting it, regardless of whether the baby is a boy or a girl.

Question 6

question: what is marfan syndrome really?

Accepted Answer

Www.marfan.org: Fibrillin-1 gene defect leads to inefficient connective tissue building.  It is inherited 70% of time. Symptoms occur in any organ that is dependent on healthy connective tissue such as the heart, lungs, skin, eyes. Marfans are tall people with thin narrow face, scoliosis, heart disease, small jaw, spidery fingers, flat feet, abnornal chest bone. You should see your dr if you suspect having it.

Question 7

what are the symptoms of marfan syndrome?

Accepted Answer

Long arms, fingers: Tall, thin appearance. Pigeon chest (pectus carinatum), long fingers (arachnodactyly), dilated aorta (seen on echocardiogram). Dislocated lens in the eye. Severe near sightedness. Scoliosis. Flat feet. High arched palate. Thin head with small cheekbones.
Most symptoms involve heart, musculoskeletal and eyes. It is inherited in an autosomal dominant fashion.

Question 8

how to figure out if i have marfan syndrome?

Accepted Answer

Testing: Physical exam and blood tests can help to determine whether you have marfan's syndrome.

Question 9

i have marfan syndrome. should i not have kids?

Accepted Answer

Maybe not: A Marfan syndrome woman has a 50% chance of having a Marfan syndrome baby, if the father of the baby is "normal". During pregnancy, the woman needs close monitoring because she is at increased risk of rupturing her aorta (often fatal). For these reasons, she may not want to become pregnant.

Question 10

does marfan syndrome disease make body thinner?

Accepted Answer

: People with Marfan syndrome are usually tall and thin with unusually long arms, legs, fingers and toes.

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