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Subtypes of EDS [view table in a new window]. Collagen is one of the main building blocks of the body. It is a protein that is widely found in all organs of the body. Several types of collagen exist, each with differing properties. Collagen can provide strength and firm support, be elastic to allow movement, or it can be used to bind things together. A genetic defect causes reduced amounts of collagen, disorganisation of collagen that is usually organised into bundles, and alterations in the size and shape of collagen. The type of EDS a patient has depends on how collagen metabolism has been affected.
See smartphone apps to check your skin. DermNet NZ does not provide an online consultation service. Although there is no cure for Ehlers-Danlos syndrome, treatment can provide symptom relief and reduce the risk of complications. People typically require physical therapy to help them manage their joint symptoms and reduce the risk of dislocations. In addition to exercises, the therapist may recommend braces or splints to provide support to weak joints.
Ehlers-Danlos syndrome tends to result in chronic pain and discomfort, often in the joints, muscles, or nerves. It can also cause stomach problems and headaches.
Medication can be a crucial part of a pain management strategy for many people with Ehlers-Danlos syndrome. For daily management, people may take over-the-counter pain reliever medications, such as acetaminophen Tylenol or ibuprofen Advil, Motrin. Acute injuries may require prescription pain relievers. A doctor may prescribe other medications for additional symptoms. For example, people with vEDS may need blood pressure-lowering medications to reduce the risk of ruptured blood vessels.
However, due to the skin symptoms that Ehlers-Danlos syndrome causes, such as slow healing, surgery poses additional risks. Living with Ehlers-Danlos syndrome poses unique challenges, and people with the condition can benefit from the support of others.
Ocular Manifestations of Ehlers-Danlos Syndrome
The outlook for Ehlers-Danlos syndrome varies among individuals, depending on the type they have and the severity of their symptoms. Aside from the vascular type, most types of Ehlers-Danlos syndrome rarely reduce life expectancy. People with vEDS have a higher risk of organ or blood vessel rupture, but taking precautions and getting the right treatment can help. For example, the authors of a long-term study reported that the participants with vEDS who received celiprolol, a blood pressure-lowering medication, had a high survival rate and a low yearly occurrence of arterial complications.
Although Ehlers-Danlos syndrome can cause uncomfortable symptoms, lifestyle changes and medical treatments can provide relief, improve quality of life, and reduce the risk of injury and complications. Article last reviewed by Wed 17 July Visit our Genetics category page for the latest news on this subject, or sign up to our newsletter to receive the latest updates on Genetics.
All references are available in the References tab. Cooley, J. Spontaneous pneumothorax in diffuse cystic lung diseases. Ehlers-Danlos syndrome. Ehlers Danlos syndromes. Ehlers-Danlos syndromes. Frank, M. Vascular Ehlers-Danlos syndrome: Long-term observational study. What are the Ehlers-Danlos syndromes? MLA Leonard, Jayne. MediLexicon, Intl. APA Leonard, J.
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Ehlers-Danlos syndrome and Marfan syndrome
Email an article. You have chosen to share the following article: How elderberries can help you fight the flu To proceed, simply complete the form below, and a link to the article will be sent by email on your behalf. Send securely. Message sent successfully The details of this article have been emailed on your behalf. By Jayne Leonard. Reviewed by Stacy Sampson, DO. Image credit: Dagger, Image credit: SamuelEDS94, Vascular EDS.
Ehlers–Danlos syndromes - Wikipedia
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