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Patients are physically underdeveloped. In 20% of patients, congenital anomalies of bones, teeth, and hair are observed. The nails are usually deformed, hypertrophied like oni-chogryphosis, or sometimes completely absent (anonychia). On atrophic deforming scars, multiple milium-like cysts are formed. Along with skin changes in patients,Xia and other manifestations of the dysplastic process: hypotrichosis, xeroderma, hypoplasia of the esophagus, gonads. At the same time, mental underdevelopment (imbecility)

Causes of epidermolysis bullosa. In addition to the easy formation of blisters and erosions, it is also characterized by increased fragility of the skin and a more severe course.

The dystrophic type of epidermolysis bullosa is caused by mutations in the COL7A1 gene, which can be inherited both by autosomal dominant and autosomal recessive mechanisms. In this case, the target protein is type 7 collagen, which is responsible for the stability of the structure of other connective tissue fibers of avodart pill.

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