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- Marfan syndrome - Symptoms and causes - Mayo Clinic
Marfan syndrome is an inherited disorder that affects connective tissue — the fibers that support and anchor your organs and other structures in your body Marfan syndrome most commonly affects the heart, eyes, blood vessels and skeleton
- Marfan Syndrome - Marfan Foundation
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
- Marfan syndrome - Wikipedia
Marfan syndrome (MFS) is a multi-systemic genetic disorder that affects the connective tissue [6] [7] [1] Those with the condition tend to be tall and thin, with long arms, legs, fingers, and toes [1] They also typically have exceptionally flexible joints and abnormally curved spines [1]
- Marfan Syndrome: Symptoms, Causes Treatment - Cleveland Clinic
Symptoms of Marfan syndrome The two main features of Marfan syndrome are aortic root aneurysm (widening or bulging of your aorta near your aortic valve) and dislocated eye lens (ectopia lentis) These two issues can lead to symptoms like: A heartbeat that feels like it’s skipping a beat or fluttering (heart palpitations)
- Marfan Syndrome Symptoms Cause | NIAMS
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
- About Marfan Syndrome | Heart Disease | CDC
Marfan syndrome is a genetic condition that affects connective tissue, which provides support for the body and organs Marfan syndrome can damage the blood vessels, heart, eyes, skin, lungs, and the bones of the hips, spine, feet, and rib cage
- Marfan Syndrome - StatPearls - NCBI Bookshelf
One of the most common inherited disorders affecting connective tissue, Marfan syndrome (MFS), is an autosomal dominant condition with a reported incidence of 1 in 3000 to 5000 individuals The defect is in the FBN1 gene of chromosome 15, which produces fibrillin, a connective tissue protein
- Marfan Syndrome: Causes, Symptoms, Diagnosis, and Treatments
Marfan syndrome affects the connective tissue in multiple parts of the body Learn more in WebMD's guide to Marfan syndrome, an inherited disease that affects the heart
- Marfan Syndrome: Symptoms, Treatment, Life Expectancy
Marfan syndrome is a genetic disease affecting the body's connective tissues, causing problems with the heart and blood vessels, eyes, and bones
- Marfan Syndrome - Harvard Health
Marfan syndrome is a genetic (inherited) disorder that affects the body's connective tissue Connective tissue is the tough, fibrous, elastic tissue that connects one part of the body with another It is a major part of tendons, ligaments, bones, cartilage and the walls of large blood vessels
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