The syndrome of Ehlers-Danlos (EDS) is the name given to a group of disorders héritables of connective fabric. This disorders characterized by defects of principal structural protein in the body (collagenous). There are seven types of EDS based on various gene changes affecting the structure or the whole of different collagens. The syndrome of Ehlers-Danlos is rare and occurs in six principal types. They can extend from soft to representative a danger to the life. Some of the symptoms more in front of the syndrome of Ehlers-Danlos include the flexible joints which are prolonged beyond normal mobility, and the that of skin particularly extensible or fragile.

Each sub-type of EDS is a distinct hereditary disorder which can assign individuals at certain families (kindreds). Approximately 1 in 5.000 people has EDS. The family history is a factor of risk in certain cases. Males and the females are also affected by the dominant recessive forms and autosomal autosomal of the syndrome of Ehlers-Danlos (EDS). In much of individuals with EDS, the associated symptoms and results can become obvious during childhood. EDS affects usually your skin, joints and walls of blood vessel. The symptoms include the loose joints, fragile and small blood vessels, abnormal formation of scar and wound the skin curative and soft, velvety, extensible which meurtrit easily.

There is no specific treatment for the syndrome of Ehlers-Danlos. The surgery is sometimes required to repair joints damaged by repeated dislocations. Isn't elective of surgery recommended. Common stability can be improved by the prescribed programs of exercise which reinforce the muscles. But avoid weightlifting. The genetic consultation will be of advantage for the individuals and the affected members of family. The other treatment for individuals with EDS is symptomatic and of support. Moreover, the physical and professional techniques specialized of therapy can help to preserve the joints and to reinforce muscles.

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