Autoimmune polyendocrine syndrome historical perspective: Difference between revisions

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Revision as of 18:39, 11 September 2017

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

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 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.

@@ Line 10: / Line 10: @@
 *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 1981, Neufeld and colleagues categorised autoimmune polyendocrine syndrome into type 1 and type 2.
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