To find out more about EDS UK, click here. They work to minimise the impact of EDS by making its diagnosis, treatment and management accessible to everyone when they need it. Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. To find out more about the Ehlers-Danlos Syndromes, including Type 3, click here.Įhlers-Danlos Support UK (EDS UK) was set up in 1987 to support, advise and inform those living with the Ehlers-Danlos syndromes. Over 30 years later, they are the largest UK charity that exclusively represents and supports people with all types of EDS. EhlersDanlos syndromes (EDS) are a group of thirteen genetic connective-tissue disorders that are in the current classification, with a fourteenth type discovered in 2018. Such problems and their severity vary considerably from person to person, even in the same type of EDS and within the same family. Symptoms commonly include, but are not limited to, long-term pain, chronic fatigue, dizziness, palpitations and digestive disorders.
These are complex syndromes affecting many systems of the body at once, despite this EDS is often an invisible disability.
As collagen is present throughout the body, people with EDS tend to experience a broad range of symptoms, most of them less visible than the skin and joint differences. This stretchiness can sometimes be seen in the skin of someone with EDS individuals with the condition may also be able to extend their joints further than is usual – this is known as being hypermobile, bendy or double-jointed. The significance of neurological findings of EDS have been recently proposed and reviewed Voermans et al., 2009a Savasta et al., 2011 Castori and Voermans, 2014. The skin sags and wrinkles, and extra (redundant) folds of skin may be. People with this form of Ehlers-Danlos syndrome have soft, doughy skin that is very fragile and bruises easily. In EDS, a gene mutation causes a certain kind of connective tissue – the kind will depend on the type of EDS but usually a form of collagen – to be fragile and stretchy. The EhlersDanlos syndromes (EDS) are a heterogeneous group of heritable connective tissue disorders characterized by joint hypermobility, skin extensibility, and tissue fragility. Ehlers-Danlos syndrome, dermatosparaxis type: A genetic disorder characterized by extremely fragile and sagging skin caused by mutation in the ADAMTS2 gene. Connective tissue lies between other tissues and organs, keeping these separate whilst connecting them, holding everything in place and providing support, like the mortar between bricks.
She also has low muscle tone which causes her to be very unsteady on her feet. The Ehlers-Danlos syndromes (EDS) are a group of thirteen individual genetic conditions, all of which affect the body’s connective tissue. Heidi has a disorder known as Ehlers Danlos syndrome type 3 a collagen disorder that makes her joints partial to sublux (dislocate) and to fully dislocate.