239 top medical experts on Hyper-IgM Immunodeficiency Syndrome across 35 countries and 15 U.S. states, including 91 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hyper-IgM Immunodeficiency Syndrome: A rare inherited immunodeficiency syndrome characterized by normal or elevated serum immunoglobulin M levels with absence of immunoglobulin G; immunoglobulin A; and immunoglobulin E. It results in a profound susceptibility to bacterial infections and an increased susceptibility to opportunistic infections. Several subtypes of hyper-IgM immunodeficiency syndrome exist depending upon the location of genetic mutation.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Genetic Diseases (2,477), Primary Immunodeficiency Diseases (1,145), Dysgammaglobulinemia (205) and Narrower Categories: Type 1 Hyper-IgM Immunodeficiency Syndrome (315).
  4. Clinical Trials ClinicalTrials.gov : at least 9 including 5 Completed, 1 Recruiting
  5. Synonyms: Type 2 Hyper-IgM Immunodeficiency Syndrome,  Type 3 Hyper-IgM Immunodeficiency Syndrome,  Type 5 Hyper-IgM Immunodeficiency Syndrome


  

        

                    


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