434 top medical experts on Autoimmune Polyendocrinopathies across 51 countries and 34 U.S. states, including 252 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Autoimmune Polyendocrinopathies: Autoimmune diseases affecting multiple endocrine organs. Type I is characterized by childhood onset and chronic mucocutaneous candidiasis (candidiasis, chronic mucocutaneous), while type II exhibits any combination of adrenal insufficiency (addison'S disease), lymphocytic thyroiditis (thyroiditis, autoimmune;), hypoparathyroidism; and gonadal failure. In both types organ-specific antibodies against a variety of endocrine glands have been detected. The type II syndrome differs from type I in that it is associated with HLA-A1 and B8 haplotypes, onset is usually in adulthood, and candidiasis is not present.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Autoimmune Diseases (3,976), Endocrine System Diseases (4,468).
  4. Clinical Trials ClinicalTrials.gov : at least 5 including 2 Completed, 2 Recruiting
  5. Synonyms: Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy,  Polyglandular Autoimmune Syndrome Type I,  Polyglandular Autoimmune Syndrome Type II,  Polyglandular Type I Autoimmune Syndrome,  Polyglandular Type II Autoimmune Syndrome,  Schmidt's Syndrome


  

        

                    


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