Localized Epidermolysis Bullosa

It is possible that the primary title of the report Epidermolysis Bullosa is not the name you expected. Please check the synonyms detailing to discover the alternating name(s) and disorder subdivision(s) covered by this report.


  • EB

Disorder Communities

  • epidermolysis bullosa simplex
  • junctional epidermolysis bullosa
  • dystrophic epidermolysis bullosa
  • Kindler disorder

General Discussion
Epidermolysis bullosa (EB) is a hereditary skin problem identified medically by sore formation from mechanical injury. There are 4 primary types with added sub-types recognized. There is a spectrum of seriousness, and within each type, one could be either mildly or badly affected. EB varies from being a minor trouble requiring modification of some tasks, to being completely disabling as well as, sometimes, deadly.

Rubbing causes sore formation. Blisters could develop anywhere on the surface of the skin, within the oral cavity and in more severe kinds may likewise entail the exterior surface area of the eye, as well as the respiratory, intestinal and genitourinary tracts. In some forms of the disease, damaging scars and disabling musculoskeletal defects occur.

Presently, there is no treatment for EB. Supportive care includes day-to-day injury care, bandaging, and discomfort management as needed.

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