200 top medical experts on Erythrokeratodermia Variabilis across 16 countries and 5 U.S. states, including 20 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Erythrokeratodermia Variabilis: An autosomal dominant skin disease characterized by transient and variable noninflammatory erythema and hyperkeratosis. It has been associated with mutations in the genes that code for connexins. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop palmoplantar keratoderma.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Erythema (1,271), Genetic Skin Diseases (3,548), Keratosis (2,394).
  4. Synonyms: Erythrokeratodermia Figurata Variabilis,  Greither Disease,  Mendes De Costa Syndrome


  

        

                    


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