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 of | *In 1929, Thorpe and Handley first described the case of mucocutaneous candidiasis with glandular failure in a 4.5-year-old girl. | ||
*In 1956, Roitt and Doniach found that patients with Hashimoto's thyroiditis had circulating autoantibodies reacting with thyroid gland. | |||
*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 18:32, 26 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 mucocutaneous candidiasis with glandular failure in a 4.5-year-old girl.
- In 1956, Roitt and Doniach found that patients with Hashimoto's thyroiditis had circulating autoantibodies reacting with thyroid gland.
- In 1981, Neufeld and colleagues categorised autoimmune polyendocrine syndrome into type 1 and type 2.