Marfan Sydrome

One can find information on marfan on its official website. Marfan syndrome is a disorder that affects connective tissue. It is usually passed from parent to child through genes.

Yes, because this syndrome is inherited.

Low visions ( weak eyes), Weak heart, weak artery, etc.

Being active! As long as you don't "force" with the exercising. You have to know when to stop playing. You can also be flexible too!

Marfan syndrome does not affect IQ.

On the contrary, people with Marfan syndrome tend to have above average intelligence. A study found that the average IQ of people with Marfans is 109.3, significantly higher than other people.

It is a genetic disorder and if one parent has it, there is a 50?50 chance that the child will have it.

Marfan syndrome affects both men and women equally, as it is inherited in an autosomal dominant manner. However, some studies suggest that men may experience more severe manifestations of the condition compared to women. Overall, the prevalence of Marfan syndrome is similar in both genders.

flat feet an sinked chest are some symptomes of marfan syndrome

you get it from one gene from your family

Marfan syndrome is commonly referred to simply as "Marfan's" or "Marfan's syndrome." It is also sometimes described in relation to its characteristics, such as "connective tissue disorder" or "hereditary connective tissue disorder." Additionally, it may be associated with specific features like "tall stature syndrome" due to the characteristic height of individuals affected by the condition.

Marfan syndrome varies in severity due to the nature of the genetic mutation affecting the FBN1 gene, which encodes fibrillin-1, a protein essential for connective tissue structure and function. The specific mutation can influence the amount and functionality of fibrillin-1 produced, leading to a range of symptoms and complications. Additionally, variable expression of the gene and differences in individual patient factors, such as other genetic modifiers and environmental influences, can further contribute to the diverse clinical manifestations observed in those with Marfan syndrome.

1 in 5,000 people.

Retinal detachment. Patients with Marfan are more vulnerable to this disorder because of the weakness of their connective tissues.

Patients with Marfan sometimes develop dental problems related to crowding of the teeth caused by a high-arched palate. They can also develop overgrowth and inflammation of the gums, due to those being part of our connective tissue.

Although protrusio acetabulae does not cause problems during childhood and adolescence, it can lead to a painful form of arthritis in adult life.

Many people respond with guilt, fear, or blame when a genetic disorder is diagnosed in the family, or they may overprotect the affected member.

In terms of the cardiac examination, a standard electrocardiogram (EKG) is not sufficient for diagnosis; only the echocardiogram can detect possible enlargement of the aorta.

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.

Smoking is particularly harmful for Marfan patients because it increases their risk of emphysema.

Marfan Syndrome is a medical problem with the Conective Tissue.

It is caused by a mutation in the gene for fibrillin-1 on chromosone 15. A variable disorder of the connective tissue that effects many organ systems including the skeleton.eyes,heart,lungs and blood vessels.