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Know more about the Marfan Syndrome ...

What is Marfan Syndrome?

This rare disorder was discovered in 1896, by a French doctor named Antoine Marfan. It is an inherited connective tissue disorder that can affect many different parts of the body. Connective tissue is made up of proteins that act like glue to support your bones, blood vessels, nervous system, skin and internal organs. Individuals suffering from Marfan Syndrome have an abnormal biochemical makeup. The connective tissue in their bodies is not as stiff as it should be which affects the growth and development of their body.

Marfan Family

Marfan FamilyMarfan syndrome is a rare disease and affects men, women and children all over the world, regardless of their age, race or ethnic background. Studies show that at least 1 out of every 5,000 people worldwide have been diagnosed with Marfan Syndrome. Approximately 60,000 to 200,000 Americans currently suffer from this disease. The disease is usually hereditary, but this is not always the case.

This photograph from 1931 shows a German family affected by Marfan Syndrome.

 

Marfan Symptoms

Main Symptoms :
  • tall
  • long narrow face
  • long arms and legs
  • possible problems
    with other organs

Marfan Syndrome can often be difficult to diagnose because the symptoms can vary greatly.  Some individuals will display very few symptoms, whereas others with more severe cases may experience life-threatening complications.  Some individuals will display symptoms at birth.  Others may not develop noticeable symptoms until much later in life. Read mor about Marfan Syndrome Symptoms...

Last updated: June 12, 2007