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.