338 top medical experts on Epidermolysis Bullosa Dystrophica across 48 countries and 22 U.S. states, including 169 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Epidermolysis Bullosa Dystrophica: Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in collagen type VII, a major component fibrils of basement membrane and epidermis.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Epidermolysis Bullosa (2,065), Collagen Diseases (842).
  4. Clinical Trials ClinicalTrials.gov : at least 55 including 9 Active, 14 Completed, 11 Recruiting
  5. Synonyms: Cockayne-Touraine Disease,  Dystrophic Epidermolysis Bullosa,  Hallopeau-Siemens Disease


  

        

                    


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