Ehlers Danlos Syndrome
Ehlers-Danlos syndrome is a group of disorders characterized by easy staining, loose joints, skin hyperelasticity and weak spot of tissues. These disorders are hereditary and effect from out of order connective tissue which affects the skin, tendons, muscles and blood vessels.
Ehlers Danlos Syndrome
Ehlers-Danlos Syndrome (EDS) (in addition known since “Cutis hyperelastica” is a group of inherited connective tissue disorders, caused by a defect in the synthesis of collagen (a protein in connective tissue). The collagen in connective tissue helps tissues to resist deformation (decreases its elasticity). In the skin, muscles, ligaments, blood vessels, and visceral organs collagen plays a very important role and with increased flexibility, secondary to abnormal collagen, pathology results. Depending on the human being mutation, the severity of the syndrome may possibly vary from mild to life-threatening. There is no cure and treatment is supportive, including close monitoring of cardiovascular system.
Signs vary widely based on which type of Ehlers Danlos Syndrome the patient has. In each example, however, the signs are finally due to faulty or reduced amounts of Type III collagen. EDS most normally affects the joints, skin, and blood vessels, the major signs and symptoms.
The Ayurvedic cure of this circumstance is aimed at treating the symptoms and attempting to turn around the basic pathology of the illness.
People affected with Ehlers-Danlos syndrome need to adopt suitable life-style modifications in order to adjust to their condition. Familiar exercise in moderation is not compulsory in order to strengthen the muscles that encourage the joints and thereby reduce joint injury. Contact sports should be avoided. It is equally critical to protect the skin from trauma and excessive exposure to the sun.