
Ehlers-Danlos syndrome - Symptoms and causes - Mayo Clinic
2022年8月25日 · Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body.
Ehlers-Danlos syndrome, type 3 - NIH Genetic Testing Registry …
Hypermobile Ehlers-Danlos syndrome (hEDS) is characterized by generalized joint hypermobility, joint instability, pain, soft and hyperextensible skin with atrophic scars and easy bruising, dental crowding, abdominal hernias, pelvic organ prolapse, marfanoid body habitus, mitral valve prolapse, and aortic root dilatation.
Ehlers-Danlos Syndrome: Symptoms, Causes & Treatment - Cleveland Clinic
2023年6月16日 · Ehlers-Danlos syndrome is a genetic condition that makes your body’s connective tissue weaker than it should be. It commonly affects your skin and joints. There’s no cure, but your healthcare provider will help you find treatments to manage your symptoms and prevent potentially dangerous complications.
Hypermobile Ehlers-Danlos Syndrome - GeneReviews® - NCBI Bookshelf
2004年10月22日 · Hypermobile Ehlers-Danlos syndrome (hEDS) is characterized by generalized joint hypermobility, joint instability, pain, soft and hyperextensible skin with atrophic scars and easy bruising, dental crowding, abdominal hernias, pelvic organ prolapse, marfanoid body habitus, mitral valve prolapse, and aortic root dilatation.
Ehlers–Danlos syndrome - Wikipedia
Ehlers–Danlos syndromes (EDS) are a group of 13 genetic connective-tissue disorders. [7] . Symptoms often include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. [1] . These may be noticed at birth or in early childhood. [3] .
Ehlers-Danlos Syndrome: Symptoms, Diagnosis, Treatment - WebMD
2024年4月9日 · Ehlers-Danlos syndrome (EDS) is an inherited condition that weakens your connective tissues, which hold parts of your body together. These include your bones and cartilage, as well as your...
What is EDS? - The Ehlers Danlos Society
Hypermobile EDS (hEDS) is the most common type of EDS by far. hEDS accounts for about 90% of EDS cases and is thought to affect at least 1 in 3,100-5,000 people. hEDS is currently classified as a rare disorder, but the true prevalence is not known and may be underestimated.
Ehlers-Danlos syndrome, type 3 (EDS3; EDSHMB) - National …
Hypermobile Ehlers-Danlos syndrome (hEDS) is characterized by generalized joint hypermobility, joint instability, pain, soft and hyperextensible skin with atrophic scars and easy bruising, dental crowding, abdominal hernias, pelvic organ prolapse, marfanoid body habitus, mitral valve prolapse, and aortic root dilatation.
hEDS - The Ehlers Danlos Society
Hypermobile Ehlers-Danlos syndrome (hEDS) is a heritable connective tissue disorder that causes generalized joint hypermobility, joint instability, and chronic pain. hEDS is also associated with a variety of other symptoms and related conditions that …
Hypermobile EDS and hypermobility spectrum disorders
Hypermobile Ehlers-Danlos syndrome (hEDS), which used to be known as the hypermobility type or type 3, is thought to be the most common genetic connective tissue disorder. There is no up-to-date research to tell us exactly how frequently it occurs.