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 |