It is recommended that patients have an echocardiogram during each of the three trimesters of pregnancy.
A pregnant woman with Marfan should also receive genetic counseling regarding the 50% risk of having a child with the syndrome.
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.
Children diagnosed with Marfan should be checked for scoliosis by their pediatricians at each annual physical examination.
Yes, Marfan syndrome is autosomal dominant.
Marfan Syndrome is a medical problem with the Conective Tissue.
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
Marfan syndrome can often be suspected based on physical features and symptoms, such as tall stature, long limbs, and joint hypermobility, but a definitive diagnosis typically requires genetic testing. Medical evaluation by a healthcare professional, including a thorough family history and assessments of the heart, eyes, and skeleton, is necessary for an accurate diagnosis. If you suspect someone has Marfan syndrome, it's important for them to seek medical advice for proper evaluation and management.
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.
They cant exercise as vigorously as someone without Marfan syndrome
flat feet an sinked chest are some symptomes of 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.