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Dec 6, 2023 · Most people with Marfan syndrome are very tall with a slim build. They usually have long extremities and long fingers and toes. People with Marfan syndrome tend to have certain other physical features as well, like a long narrow skull, deep-set eyes, and an abnormally small jaw.
Jun 3, 2022 · Marfan syndrome (also called Marfan’s syndrome or Marfans syndrome) is a condition that affects your connective tissue. Connective tissue holds your body together and provides support to many structures throughout your body. In Marfan syndrome, the connective tissue isn’t normal.
Marfan syndrome is a rare genetic disorder of the connective tissue, affecting the skeleton, lungs, eyes, heart and blood vessels. The condition is caused by a defect in the gene that tells the body how to make fibrillin-1, often from a parent who is also affected.
Feb 24, 2020 · Marfan syndrome is a genetic condition that affects connective tissue, which plays a crucial role in forming skin, bones, blood vessels, the heart, and other vital organs.
Marfan syndrome is caused by a defect (or mutation) in the gene that tells the body how to make fibrillin-1. This mutation results in an increase in a protein called transforming growth factor beta, or TGF-β.
Aug 14, 2022 · 7 min read. What Is Marfan Syndrome? Marfan syndrome is an inherited disease that affects your body's connective tissue, which gives strength, support, and elasticity to tendons,...
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Overview, Symptoms, & Causes. Diagnosis, Treatment, & Steps to Take. More Info. Overview of Marfan Syndrome. Marfan syndrome is a genetic disorder that changes the proteins that help make healthy connective tissue. This leads to problems with the development of connective tissue, which supports the bones, muscles, organs, and tissues in your body.
