Autoimmune polyendocrine syndrome historical perspective: Difference between revisions

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*In 19th century physicians first focussed their attention on constellation of symptoms associated with autoimmune polyendocrine syndrome.
*In 19th century physicians first focussed their attention on constellation of symptoms associated with autoimmune polyendocrine syndrome.
*In 1855, Thomas Addison identified patients with Addison's disease who also appeared to have coexisting pernicious anemia.
*In 1855, Thomas Addison identified patients with Addison's disease who also appeared to have coexisting pernicious anemia.
*In 1929, Thorpe and Handley first described the case in a 4.5-year-old girl with mucocutaneous candidiasis with glandular failure.
*In 1929, Thorpe and Handley first described the case of autoimmune polyendocrine syndrome in a 4.5-year-old girl with mucocutaneous candidiasis with glandular failure.
*In 1981, Neufeld and colleagues categorised autoimmune polyendocrine syndrome into type 1 and type 2.
*In 1981, Neufeld and colleagues categorised autoimmune polyendocrine syndrome into type 1 and type 2.



Revision as of 12:26, 22 September 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

Historical Perspective

  • In 19th century physicians first focussed their attention on constellation of symptoms associated with autoimmune polyendocrine syndrome.
  • In 1855, Thomas Addison identified patients with Addison's disease who also appeared to have coexisting pernicious anemia.
  • In 1929, Thorpe and Handley first described the case of autoimmune polyendocrine syndrome in a 4.5-year-old girl with mucocutaneous candidiasis with glandular failure.
  • In 1981, Neufeld and colleagues categorised autoimmune polyendocrine syndrome into type 1 and type 2.

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