What are the symptoms of Ehlers-Danlos syndrome?
The symptoms of Ehlers-Danlos (EDS) syndrome are primarily associated with abnormal collagen and affected joints, walls of blood vessels and skin. Having very flexible or free joints and stretching skin are two of the most important symptoms of Ehlers-Danlos syndrome, although the double clutch is not the same as having syndrome. There are several types of ED, each with its own specific set of symptoms: classic type, type of hypermobility and vascular type. EDS is an unusual syndrome. The skin will be very soft, easily bruised or damaged and extremely elastic. In addition, a person with EDS can be a flat foot and a scar easily. The classic type is characterized by free joints, elastic skin and redundant skin folds. The wounds are slowly recovering and growth on the elbows and knees and thermal valve techniques are other signs of this type of ED. The skin is so thin that it is almost translucent and easily bruise. The patient's face includes thin nose and lips, small chin and recessed faces. Packed lungs are another symptom of EDS vascular type.
A person with a type of hypermobility ED will have free and unstable joints that are often dislocated. He or she will also experience muscle fatigue, premature osteoarthritis and chronic degenerative joint disease. There are other ED types, but they are so rare that they have been diagnosed in only a few families.
Genetic mutations passing from parent to child cause all ED types. These mutations interrupt the production of collagen, a protein that makes the connective tissues strong and elastic. As a result, these tissues can become unstable and weak.
EDS diagnosis usually begins with complete physical examination. Very loose joints and stretched and fragile skin associated with a family history of disorders usually sufficient to make a diagnosis. Further testing, such as genetic tests, skin biopsy or echocardiogram, can be ordered to help determine the specific ED type.
Possibilities of treatment pThey are going to manage their symptoms of Ehlers-Danlos syndrome, but there is no treatment. Strengthening muscles by physical therapy can stabilize joints and reduce muscle pain. Surgery is recommended for repairing the damaged joint, but the syndrome can be complicated because the stitches do not have to hold the elastic skin together. Local anesthetics and non -steroidal anti -inflammatory drugs can be prescribed for muscle and joint pain.
patients with symptoms of Ehlers-Danlos syndrome should work to protect their skin and joints from injury. Contact Sportsa weightlifting may not be suitable activities for people with EDS. Protective equipment and auxiliary equipment can reduce joint stress. The use of sunscreen and mild soaps will help protect easily damaged skin. People with EDS can consider it beneficial to build a support system and explain their symptoms to friends, family and their employers.
Mental function is not affected by the symptoms of ehlers-danlos syndrome, although complications may limitphysical activity. Such complications may include scarring, chronic pain and joint dislocation and arthritis of timely onset. Women with ED who want to conceive should consult with their doctors or genetic advisor before conception.