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Marfan's Syndrome
Marfan syndrome is an inherited disorder of the connective tissue (tissue that provides the support for the skeletal structure and all organs of the body) that affects normal body growth. More »
Source: healthline.com

Marfan syndrome - Wikipedia


Marfan syndrome (MFS) is a genetic disorder of the connective tissue. The degree to which people are affected varies. People with Marfan tend to be tall, and ...

What is Marfan Syndrome? | The Marfan Foundation


Marfan syndrome is a genetic disorder that affects the body's connective tissue. Connective tissue holds all the body's cells, organs and tissue together. It also ...

What are the signs? | The Marfan Foundation


Knowing the signs of Marfan syndrome can save livesPeople are born with Marfan syndrome and related disorders, but they may not notice any features until ...

Marfan syndrome - Genetics Home Reference


Marfan syndrome is a disorder that affects the connective tissue in many parts of the body. Connective tissue provides strength and flexibility to structures such ...

Marfan Syndrome Symptoms, Causes, Treatments - WebMD


Feb 16, 2016 ... WebMD's guide to Marfan syndrome, an inherited disease that affects the heart.

Overview - Marfan syndrome - Mayo Clinic


Mar 10, 2016 ... Marfan syndrome is an inherited disorder that affects connective tissue — the fibers that support and anchor your organs and other structures in ...

Marfan Syndrome: MedlinePlus


Jul 13, 2016 ... Marfan syndrome is a disorder that affects connective tissue. Marfan syndrome can be mild to severe. Read about symptoms and outlook.

Learning About Marfan Syndrome - National Human Genome ...


There is a wide variability in clinical symptoms in Marfan syndrome with the most notable occurring in eye, skeleton, connective tissue and cardiovascular ...

Genetics of Marfan Syndrome: Background, Pathophysiology ...


Jan 4, 2017 ... Marfan syndrome (MFS) is an inherited connective tissue disorder, noteworthy for its worldwide distribution, relatively high prevalence, and ...