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. 2022 Apr 4;14(2):62–64. doi: 10.4103/ijt.ijt_77_20

Table 1.

Classification of autoimmune polyglandular syndromes

PAS type Characteristics
Juvenile
 Type I Chronic candidiasis, chronic hypoparathyroidism, and Addison’s disease (at least two present)
Adult
 Type II Addison’s disease (always present), autoimmune thyroid disease and/or diabetes mellitus Type I
 Type III Autoimmune thyroid disease associated with another autoimmune disease (excluding Addison’s disease and/or hypoparathyroidism)
  IIIA APS Type III + endocrine diseases
  IIIB APS Type III + gastrointestinal or hepatic autoimmune diseases
  IIIC APS Type III + skin or neuromuscular or nervous system autoimmune diseases
  IIID APS Type III + collagen diseases, vasculitis, or hematologic autoimmune diseases
  Type IV Combinations of glandular autoimmune diseases that are not included in the previous groups