Ehlers danlos syndrome symptoms

What is the life expectancy of someone with Ehlers Danlos? Does Ehlers Danlos have a cure? Can people with Ehlers Danlos work? Is Ehlers Danlos an autoimmune disease?

Because the connective tissue that holds joints together is looser,. Weakened connective tissue allows your skin to stretch much more than usual.

Ehlers-Danlos syndrome (EDS) is an inherited condition that affects the connective tissues in the body. Connective tissue is responsible for supporting and structuring the skin, blood vessels. The most common form of EDS makes your joints bend farther than they. Chronic , early onset, debilitating musculoskeletal. When the connective tissue is faulty, it can cause joints to sublux or dislocate completely and can make the skin stretchy and fragile.

These can be noticed at birth or in early childhood. Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis. If your patients have EDS, use these tools to screen for narcolepsy symptoms.

When the skin is damage the healing process will usually take a great deal of time.

Overly Flexible Joints. Ehlers - Danlos syndrome patients have weakened connective tissues,. Delicate, small blood vessels. Stretchy skin that is soft or velvety.

Frequent, unusual scarring. In EDSpatients, though, they are usually subtle. Subcutaneous veins are visible. Soft, velvety skin stretches excessively but returns to normal after being pulled.

Some forms of EDS can present problems with the spine,. The Research Portfolio Online Reporting Tool (RePORT) provides access to reports, data, and analyses of research activities at the National Institutes of Health (NIH), including information on NIH expenditures and the of NIH-supported research. Cardiac-valvular type (cvEDS) cvEDS is a rare subtype of EDS wherein patients may have minor signs of EDS with severe defects to their aorta, requiring surgical interventions. Vascular type (vEDS) vEDS (formerly EDSIV), can be identified at birth with noticeable clubfoot deformities and dislocation of the hips.

They are generally characterized by joint hypermobility (joints that stretch further than normal), skin hyperextensibility (skin that can be stretched further than normal), and tissue fragility. The cardiac-valvular type causes severe problems with the valves that control the movement of blood through the heart. Skin may become fragile and bruises easily. Joint pain and dislocations are common. If the skin is damage it often doesn’t heal well.

Vascular Ehlers-Danlos Syndrome (vEDS) This is one of the most severe Ehlers-Danlos Syndrome types.

The skin of someone with EDS may feel very soft and velvety. Those with vEDS can suffer from weakened or ruptured arteries and blood vessels including the aorta (the heart’s largest artery) and arteries that move blood through the kidneys and spleen. Each of the different types of Ehlers Danlos syndrome is associated with different genetic causes. In some types of this medical condition, such as Vascular Ehlers Danlos syndrome , there is a fifty percent chance that the defective gene will be passed on to the children.

There are many types of Ehlers Danlos syndrome and each one is identified by unique and different symptoms. All the types however cause problems in the joints, skin, and other body areas. Patients do not experience any mental issues, but physical work may be restricted due to EDS-linked complications. The symptoms that one experiences with EDS are mostly due to the lack of collagen or issues with collagen production.

Symptoms of Ehler’s Danlos Syndrome. Therefore, not everyone will experience the same symptoms. Others have worse symptoms, and some individuals are lucky enough to only have mild harmless symptoms.