Ehlers Danlos Syndrome Type 3
Those affected have trouble with hyperflexibility as well as oddly fragile and stretchy skin.
Ehlers danlos syndrome type 3. This means that a child cannot inherit a different type of eds to the one their parent has. Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. The skin is often soft and may be mildly hyperextensible.
Hyperlaxity is a normal varia. Some of the rare, severe types can be life threatening. These are things like tendons and ligaments that hold parts of your body together.
Depending on the type of eds, the faulty gene may have been inherited from 1 parent or both parents. Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis. See more ideas about ehlers danlos syndrome, hypermobility, dysautonomia.
31 years experience orthopedic surgery. Subluxations and dislocations are common; They also have thin, translucent skin that bruises very easily.
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) Chronic pain is the most prominent symptom of ehlers danlos syndrome. The basic idea by doctors ehlers and danlos remains somewhat intact today:
Sometimes the faulty gene is not inherited, but occurs in the person for the first time. Individuals with eds demonstrate defects in the body's connective tissues, manifesting as altered strength, elasticity, integrity, and healing properties of the tissues. 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.
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