475 top medical experts on Ectodermal Dysplasia across 43 countries and 33 U.S. states, including 363 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Ectodermal Dysplasia: A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, focal dermal hypoplasia, and aplasia cutis congenita.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Genetic Skin Diseases (3,548), Multiple Abnormalities (3,208), Skin Abnormalities (2,933) and Narrower Categories: Anhidrotic Ectodermal Dysplasia 1 (763), Anhidrotic Ectodermal Dysplasia 3 (23), Autosomal Recessive Hypohidrotic Ectodermal Dysplasia (126), Ellis-Van Creveld Syndrome (774), Focal Dermal Hypoplasia (435), Neurocutaneous Syndromes (1,959), Pachyonychia Congenita (364).
  4. Clinical Trials ClinicalTrials.gov : at least 25 including 1 Active, 17 Completed, 3 Recruiting
  5. Synonyms: Anhidrotic Ectodermal Dysplasia,  Aplasia Cutis Congenita,  Clouston's Syndrome,  Congenital Ectodermal Defect,  Hidrotic Ectodermal Dysplasia


  

        

                    


    Computing Expert Listing ...

);