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This allows you to estimate the amount of a particular protein, which, in turn, indicates the enzymatic activity of tissues. A decrease in the amount of a particular protein indicates its low release or accelerated destruction. Reducing the concentration of key proteins in certain areas allows you to determine the level of development of blisters at a very early stage, which already helps to determine the type of epidermolysis bullosa with a high degree of probability.
Significantly simplify the diagnosis of thisdisease allows the study of mobic online hereditary history, by which it is possible to identify his blood relatives with the same problem. In addition, if one of the relatives has epidermolysis bullosa, it makes sense to perform prenatal genetic diagnosis, which will reveal the presence of this pathology in the early stages of fetal development. Differential diagnosis is carried out with true pemphigus, some forms of bullous pemphigoid, acquired epidermolysis bullosa (which is not a hereditary, but an autoimmune disease).
Treatment of bullous epidermolysis. There is no specific treatment for this disease; all therapeutic procedures are reduced to preventing the development of complications and reducing the severity of vesicles and erosions. In the case of severe forms of bullous epidermolysis, prednisolone is prescribed.
From external therapeutic manipulations, an aseptic opening of the bubbles is performed, their lids are treated with antiseptics, and heliomycin ointment is applied. Bandaging should be done with extreme caution, as the pressure of the bandages can provoke the appearance of new meloxicam blisters. In the presence of complications (shock, sepsis), symptomatic treatment with anti-shock drugs and antibiotics is carried out. For prophylactic purposes, it is possible to irradiate the skin with ultraviolet rays.
Patients with such a problem should take care of mobic pill, do not forget about the antiseptic treatment of erosions and other lesions, avoid engaging in traumatic sports and other activities of this kind. The concept of epidermolysis bullosa was introduced by the German dermatologist Heinrich Koebner as early as 1886, although similar cases of skin diseases have occurred before. Life expectancy in epidermolysis bullosa.