Abstract
Autoimmune polyglandular syndromes are groups of disorders characterized by two or more glandular autoimmune-mediated diseases. Autoimmune polyglandular syndromes can have endocrine and nonendocrinological components. There are two main types of autoimmune polyglandular syndromes, type 1 and type 2. These two processes differ on age of onset, endocrine glands affected, and genetic etiology. While these syndromes involve multiple autoimmune disease processes, the appearance of more than one autoimmune disease can take years to manifest. Treatment of these conditions should be tailored to the disease process that is present.
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