Unlike the diseases noted above, Ehlers-Danlos syndrome is not an autoimmune condition, it's an inherited disorder. Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders caused by abnormalities in the structure, production, and/or processing of collagen. These can be noticed at birth or in early childhood. A much rarer group of connective tissue disorders is called Ehlers-Danlos syndrome. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body.People who have Ehlers-Danlos syndrome usually have overly flexible joints and stretchy, fragile skin. It causes numbness, tingling or burning sensations, A sense of anxiety, tremor, and cold, sweaty hands and feet, Dark red or bluish color to the legs when standing up. COVID-19 tools and resources: symptom checker, visitor restrictions, testing info and safety measures. Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. Your HonorHealth neurologist will first complete a personal and family medical history and conduct an exam. Although there's no cure, there are treatment options for symptoms caused by Ehlers-Danlos syndrome. In the United States, two million people live with rheumatoid arthritis, and another 1.5 million live with lupus. Ehlers-Danlos syndrome (EDS) is an inherited condition that affects the connective tissues in the body. What is Ehlers-Danlos syndrome? Ehlers-Danlos syndrome can take one of several forms and is believed to affect 1.5 million people around the globe. There are no other risk factors. Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis. Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls. It is generally considered the least severe form of Ehlers-Danlos syndrome (EDS) although significant complications can occur. Although some rare forms of the disease are potentially life threatening, the majority of patients have a normal life expectancy. A much rarer group of connective tissue disorders is called Ehlers-Danlos syndrome.
More than 200 connective tissue diseases – inflammatory disorders of muscle, joints and skin — have been identified. Classified at the beginning of the 20th century, Ehlers-Danlos syndrome is inherited, passed from parent to child. Hypermobile Ehlers-Danlos syndrome is an inherited connective tissue disorder that is caused by defects in a protein called collagen. Ehlers-Danlos can occur as a result of inheriting affected genes from your parents. Ehlers–Danlos syndromes (EDS) are a group of rare genetic connective tissue disorders. If you have Ehlers-Danlos syndrome, your body has a problem producing collagen, making your connective tissues weaker than they should be.
Although other forms of the condition may exist, they are extremely rare and are not well-characterized. Learn more. Connective tissue is responsible for supporting and structuring the … Mutations in at least 19 genes have been linked to Ehlers-Danlos syndromes. The most common connective tissue disorders are rheumatoid arthritis and systemic lupus. Ehlers-Danlos syndrome can take one of several forms and is believed to affect 1.5 million people around the globe. Unlike the diseases noted above, Ehlers-Danlos syndrome is not an autoimmune condition, it's an inherited disorder. Your neurologist may also conduct the following tests to confirm diagnosis: Treatment often consists of medications and physical therapy. Connective tissue disease - Ehlers-Danlos syndrome, Skin that can be stretched farther than normal (skin hyperextensibility), Fragility of tissue caused by a deficiency in collagen, the primary structural protein that helps tissues stay supple, Easily bruised skin, problems with healing skin and unique scarring, Joints that stretch farther than normal (called joint hypermobility), Issues with heart valves and blood vessels for some conditions, Dysautonomia, causing light-headedness, rapid heart rate, fainting, fatigue and gastrointestinal symptoms, Temporomandibular joint pain and dysfunction, Small fiber neuropathy, a condition that affects the sensory nerves. The new classification , from 2017, includes 13 subtypes of EDS.
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