Ehlers Danlos Syndrome Type 3
Chronic pain is the most prominent symptom of ehlers danlos syndrome.
Ehlers danlos syndrome type 3. This is a video explaining the most important characteristics of this condition. Those affected have trouble with hyperflexibility as well as oddly fragile and stretchy skin. Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis.
They may occur spontaneously or with minimal trauma and can be acutely painful. See more ideas about ehlers danlos syndrome, hypermobility, dysautonomia. Subluxations and dislocations are common;
Subluxations and dislocations are common; Classical features of ehlers danlos syndrome or eds may include doughy, soft, hyper elastic skin. Frequent joint dislocations and subluxations (partial dislocation), often affecting the shoulder, kneecap, and/or temporomandibular joint (joint that connects the lower jaw to the skull)
These tissues—found mostly in the skin, joints, and blood vessel walls—act like a glue to help provide strength and elasticity to the body’s structures, including the digestive system and essential organs. Eds occurs due to variations of more than 19. The skin is often soft and may be mildly hyperextensible.
This means that a child cannot inherit a different type of eds to the one their parent has. Depending on the type of eds, the faulty gene may have been inherited from 1 parent or both parents. Individuals with eds demonstrate defects in the body's connective tissues, manifesting as altered strength, elasticity, integrity, and healing properties of the tissues.
Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. 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. Hyperlaxity is a normal varia.