Also known as: Marfan’s syndrome.
What is Marfan syndrome?
Marfan syndrome is a genetic disorder that negatively affects the connective tissue of the body. The problems caused by Marfan syndrome can lead to issues with the heart, blood vessels, muscles, bones and ligaments, among other problems.
What causes Marfan syndrome?
Marfan syndrome is caused by genetic mutations in Fibrillin gene. In most cases, it is inherited from parents and passed along to the children, though it can also occur randomly.
What are the symptoms of Marfan syndrome?
Common symptoms of Marfan syndrome include a tall, slender build with long arms, legs and fingers. These are accompanied by heart problems, nearsightedness, a curved spine (scoliosis), flat feet and other symptoms.
What are Marfan syndrome care options?
There is no cure for Marfan syndrome. Treatment is focused on preventing problems or managing them as they occur through medications, therapy and surgery.
Reviewed by: Parul B Jayakar, MD
This page was last updated on: December 18, 2020 05:06 PM