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This is the material that provides strength and structure to: Skin Bone Blood vessels Internal organs The abnormal collagen leads to the symptoms associated with EDS. Family history is a risk factor in some cases. Symptoms of EDS include: Back pain Double-jointedness Easily damaged, bruised, and stretchy skin Easy scarring and poor wound healing Flat feet Increased joint mobility, joints popping, early arthritis Joint dislocation Joint pain Premature rupture of membranes during pregnancy Very soft and velvety skin Vision problems.

Exams and Tests. Examination by a health care provider may show: Deformed surface of the eye cornea Excess joint looseness and joint hypermobility Mitral valve in the heart does not close tightly mitral valve prolapse Gum infection periodontitis Rupture of intestines, uterus, or eyeball seen only in vascular EDS, which is rare Soft, thin, or very stretchy skin Tests to diagnose EDS include: Collagen typing performed on a skin biopsy sample Collagen gene mutation testing Echocardiogram heart ultrasound Lysyl hydroxylase or oxidase activity to check collagen formation.

Outlook Prognosis.

People with EDS generally have a normal life span. Intelligence is normal. Possible Complications. Possible complications of EDS include: Chronic joint pain Early-onset arthritis Failure of surgical wounds to close or stitches tear out Premature rupture of membranes during pregnancy Rupture of major vessels, including a ruptured aortic aneurysm only in vascular EDS Rupture of a hollow organ such as the uterus or bowel only in vascular EDS Rupture of the eyeball. When to Contact a Medical Professional. Call for an appointment with your provider if you or your child has symptoms of EDS.

Ehlers-Danlos Syndrome Read more. Overview Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls. Request an Appointment at Mayo Clinic. Share on: Facebook Twitter. References Pauker SP, et al. Clinical manifestations and diagnosis of Ehlers-Danlos syndrome. Accessed June 29, Ferri FF. Ehlers-Danlos syndrome.

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Rare Disease Database

In: Ferri's Clinical Advisor Philadelphia, Pa. Rochester, Minn.

Your Eyes and EDS - Lecture Series

Pauker SP, et al. Overview of the management of Ehlers-Danlos syndrome. Ehlers Danlos syndrome.

National Organization for Rare Disorders. Accessed July 1, Byers PH, et al.

What causes the Ehlers Danlos syndromes?

Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome. Each type of Ehlers-Danlos Syndrome is defined as having a distinct problem in the connective tissue.

In a person with EDS, the connective tissue is not structured normally. Some of, or all of the tissue in the EDS-affected body can be stretched beyond normal limits which can lead to damage. One of the major problems with EDS is that ligaments are too lax to hold the joints correctly in place, and they may dislocate or subluxate.

The muscles are then forced to work harder to compensate, and may cause muscle spasms and trigger points myofascial pain. A body with EDS can behave unreliably, and issues can be widespread and range in severity, from barely noticeable to life-threatening. It can appear as though a person has a large number of seemingly-unrelated symptoms.

This is one reason why medical professionals not. It may take decades to get properly diagnosed. Misdiagnoses of Arthritis, Fibromyalgia and Chronic Fatigue Syndrome are common because many of the symptoms, especially joint and muscle pain, chronic fatigue , headaches, autonomic dysfunction, and other symptoms overlap with those of EDS. How common are Ehlers-Danlos Syndromes?

At this time, research statistics of the Ehlers-Danlos Syndromes show the total prevalence in patients as 1 in 2, to 1 in 5, people.

Ehlers-Danlos syndrome and Marfan syndrome – Knowledge for medical students and physicians

However, recent clinical experience suggests that Ehlers-Danlos Syndrome may actually be even more common than this. EDS affects people of all racial and ethnic backgrounds and is much more common in females than males. Many types of EDS are considered extremely rare.


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Types and severity of symptoms vary for each individual. Although some EDS symptoms can appear in infancy or early childhood, it is more common to start noticing symptoms from the teenage years. Many with EDS were once very good at sport or activities that required hypermobility e.