The Mighty’s Condition Guides combine the expertise of both the medical and patient community to help you and your loved ones on your health journeys. For the Ehlers-Danlos syndrome EDS guide, we interviewed three medical experts, read numerous studies and surveyed more than 750 people living with EDS. The guides are living documents and. Ehlers-Danlos Syndrome EDS is a complex disorder and shares overlapping symptoms with other connective-tissue disorders, as well as other common conditions. In addition, there are 13 types of EDS alone – with varying treatments. If EDS is suspected, an early confirmed diagnosis is imperative to keep the condition from getting worse. Many other conditions commonly occur alongside hypermobile EDS hEDS and hypermobility spectrum disorders HSD. Although an association has been demonstrated between hEDS/HSD and most of these problems, there is not yet enough scientific evidence to prove that one issue causes the other. This section provides information and advice on living with these comorbidities.
Documents and information submitted under the Maryland Solicitations Act for EDS Wellness are also available, for the cost of postage and copies, from the Maryland Secretary of State, State House, Annapolis MD 21401, 410 974-5534. Answers from doctors on eds medical condition. First: Most patients with narcolepsy with cataplexy have a genetic marker called hla dqb10602. However, many people without narcolepsy also this same marker. As such, simply having the marker is not sufficient to cause the condition. The current thought is that in narcolepsy an infection triggers. EDS is listed as a "rare disease" by the Office of Rare Diseases ORD of the National Institutes of Health NIH. This means that EDS, or a subtype of EDS, affects less than 200,000 people in the US population.
Ehlers-Danlos Syndrome EDS is a group of genetic disorders of the connective tissue. Ehlers-Danlos Syndrome is a constellation of many different disorders, all sharing to some degree a defect in a patient’s connective tissue that makes that tissue fragile and stretchy. This may result in complications ranging from easy bruisability, loose. Ehlers-Danlos syndrome EDS is a group of inherited conditions that affect collagen. Collagen is the material that provides strength and structure to skin, bone, blood vessels and internal organs. EDS causes loose hypermobile joints, extremely elastic skin that bruises easily and fragile blood vessels. Medical Definition of Ehlers-Danlos syndrome Medical Author: William C. Shiel Jr., MD, FACP, FACR Ehlers-Danlos syndrome: A heritable disorder of connective tissue that is characterized by easy bruising, joint hypermobility loose joints, skin laxity, and weakness of tissues. Ehlers-Danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. Defects in connective tissues cause the signs and symptoms of these conditions, which range from mildly loose joints to life-threatening complications.
Exact matches only. Exact matches only. Search in title. Conditions linked to EDS Many other conditions appear to commonly occur alongside the Ehlers-Danlos syndromes, particularly together with hypermobile EDS. People with the Ehlers-Danlos syndromes and hypermobile spectrum disorders HSD often identify themselves as zebras. Medical students have been taught for decades that, “When you hear hoofbeats behind you, don’t expect to see a zebra.”.
The condition disrupts the production of collagen, the material that provides strength and structure to skin, bone, tendons, ligaments, cartilage, blood vessels, and internal organs. There are several types of Ehlers-Danlos syndrome, but each type affects the joints, and most types affect the skin. Some forms of this condition can lead to the rupture of internal organs, abnormal heart valves, or aneurysms. Find a condition that begins with the letter Z Z; Find a disease that starts with a numberSymptom Checker. Check on one or more symptoms to find possible causes. About this Symptom Checker. First Aid Information to help you during a medical emergency. Use this voice app to get quick self-care instructions for burns, choking, insect bites and more. Try our voice app. Featured topics. Cancers. The classical type of EDS targets 1 in 20,000 to 40,000 people. That said, EDS is gravely underdiagnosed, likely due to a lack of knowledge and understanding about this condition in the medical profession, so actual numbers may be much higher.
EDS is usually suspected because you have the typical symptoms of one of the types. The doctor may ask about close family members and any problems they may have had with their skin or joints. Once the condition is suspected, specialist testing, including genetic testing, may be offered to determine which type of EDS you have.