Patients who have had a valve replaced must take an anticoagulant medication, usually warfarin (Coumadin), in order to minimize the possibility of a clot forming on the prosthetic valve.
Recent advances in Marfan syndrome treatment have prolonged the life expectancy of patients considerably. Changes in how the syndrome is treated, including medication, surgical interventions, and monitoring for complications of the syndrome (eg, aneurysms), are all responsible for the increase in life expectancy. The prolongation in life expectancy can be seen by taking a look at statistics from 1972, in which the life expectancy was 32 years, and from 1996, where patients with Marfan syndrome had a life expectancy of 61 years.
Marfan syndrome is found in 1 in every 5,000 - 10,000 births. If one of your parents has Marfan syndrome, you have a 50% chance of having Marfan syndrome.
Marfan Syndrome is a medical problem with the Conective Tissue.
Yes, Marfan syndrome is autosomal dominant.
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
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.
flat feet an sinked chest are some symptomes of marfan syndrome
They cant exercise as vigorously as someone without Marfan syndrome
Marfan syndrome is not naturally found in animals. However, researchers have created mice with Marfan syndrome in laboratories for the purpose of testing medications on them before conducting human trials.
Marfan syndrome was first described by Antoine Marfan, a French pediatrician, in 1896. He identified the unique characteristics of the syndrome, including tall stature, long limbs, and heart problems.
The etiology of marfan syndrome would be the mutations in the protein FBN1 in the gene chromosome 15.