206 top medical experts on type 1 Autoimmune polyendocrinopathy syndrome across 21 countries and 6 U.S. states, including 32 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. type 1 Autoimmune polyendocrinopathy syndrome: A rare, genetic, disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Autosomal Dominant Type I Autoimmune Polyendocrinopathy Syndrome,  With Reversible Metaphyseal Dysplasia Type I Autoimmune Polyendocrinopathy Syndrome,  type 1 Autoimmune polyendocrine syndrome,  Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED),  Hypoadrenocorticism with hypoparathyroidism and superficial moniliasis,  Persian-Jewish Type Polyglandular Deficiency Syndrome


  

        

                    


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