Yes Marfan syndrome is a dominate disorder that affects the bodies connective tissue. it also causes problems in the heart, eyes and bones
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.
Anyone can get Marfans syndrome, it is a genetic disorder.
marfan syndrome is genetic disorder of connective tissue of the body. it cause a mutation of the gene that produces the protein fibrillin.
No, Marfan Syndrome is an inherited disorder of connective tissue. It is not an infectious disease.
Marfan's syndrome is the most common genetic disorder of connective tissue. It occurs in about every 10,000 to 20,000 individuals.
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 (also called Marfan's syndrome) is a genetic disorder of the connective tissue. People with Marfan's tend to be unusually tall, with long limbs and long, thin fingers.
Marfan's syndrome is a genetic disorder, so one would inherit it from their biological parents. You can't "catch" marfans syndrome
Marfan's Syndrome is inherited in an autosomal dominant pattern. This disease is a disorder that affects the connective tissue in many parts of the body.
While there is no cure for Marfan Syndrome (because it is a genetic disorder), there are ranges of treatment options can decrease (and even sometimes prevent) complications.
Abraham Lincoln was thought to have Marfan syndrome. This has not been proven however, and many researchers think he may have had a different disorder instead.
Marfan syndrome is an autosomal dominant disorder. An affected person has a 50% chance of passing it on to each offspring, regardless of gender.