Publisher's Synopsis
INTRODUCTION TO MARFAN SYNDROME
Marfan syndrome is a rare genetic disorder that affects the body's connective tissue. This can cause defects in the heart, lungs, and spine. Marfan syndrome is most common in women, but it can also occur in men.
The cause of Marfan syndrome is unknown. However, the disorder is believed to be inherited. Marfan syndrome is usually diagnosed when a person has signs and symptoms of the disorder. These can include abnormal growths on the body (such as a winged nose or a long neck), difficulty breathing, and heart problems.
Marfan syndrome can be treated with a variety of treatments. Treatment can include surgery to correct defects in the heart, lungs, or spine. In some cases, treatment may include medication to help improve the symptoms of Marfan syndrome.
Marfan syndrome is a serious disorder, but it can be treated. If you have signs and symptoms of Marfan syndrome, please consult your doctor.
Marfan syndrome is a connective tissue disorder that affects the body's muscles and tendons. People with Marfan syndrome have a higher risk of developing heart problems, including sudden death. Marfan syndrome is a rare disorder, affecting only about 3 in 10,000 people.
There is no one cause of Marfan syndrome, but it is believed to be caused by a combination of genetics and environmental factors. Marfan syndrome is usually diagnosed in children or young adults, but it can also be diagnosed in adults.
Marfan syndrome is a serious condition, and people with Marfan syndrome need to be treated carefully. Treatment may include surgery to repair damage to the muscles and tendons and medicines to prevent heart problems.
If you are concerned about your health and want to learn more about Marfan syndrome, please visit the Marfan Foundation website or contact your doctor.