Autoimmune polyendocrine syndrome history and symptoms
Autoimmune polyendocrine syndrome Microchapters |
Differentiating Autoimmune polyendocrine syndrome from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Autoimmune polyendocrine syndrome history and symptoms On the Web |
American Roentgen Ray Society Images of Autoimmune polyendocrine syndrome history and symptoms |
FDA on Autoimmune polyendocrine syndrome history and symptoms |
CDC on Autoimmune polyendocrine syndrome history and symptoms |
Autoimmune polyendocrine syndrome history and symptoms in the news |
Blogs on Autoimmune polyendocrine syndrome history and symptoms |
Directions to Hospitals Treating Autoimmune polyendocrine syndrome |
Risk calculators and risk factors for Autoimmune polyendocrine syndrome history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
History and Symptoms
Type I: fungal infections (chronic mucocutaneous candidiasis), thyroid issues (hypoparathyroidism), autoimmune adrenal insufficency, type 1 diabetes, reproductive issues (hypogonadism), anemia, malabsorption, baldness, and vitiligo
- Symptoms may appear as young as five years old (specifically with candidiasis). Hypoparathyroidism commonly appears in people younger than 10 years. Autoimmune adrenal insufficency appears in people younger than 15 years.
Type II: autoimmune disease (Addison's disease), thyroid disease, type 1 diabetes, reproductive issues (hypogonadism), digestive issues (Celiac disease) and neuromuscular disease (myasthenia gravis). Type III: digestive issues (Celiac disease and gastric carcinoid tumors), reproductive issues (hypogonadism), autoimmune disorders (sarcoidosis), and rheumatoid arthritis.