Autoimmune polyendocrine syndrome natural history, complications and prognosis
Autoimmune polyendocrine syndrome Microchapters |
Differentiating Autoimmune polyendocrine syndrome from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Autoimmune polyendocrine syndrome natural history, complications and prognosis On the Web |
American Roentgen Ray Society Images of Autoimmune polyendocrine syndrome natural history, complications and prognosis |
FDA on Autoimmune polyendocrine syndrome natural history, complications and prognosis |
CDC on Autoimmune polyendocrine syndrome natural history, complications and prognosis |
Autoimmune polyendocrine syndrome natural history, complications and prognosis in the news |
Blogs on Autoimmune polyendocrine syndrome natural history, complications and prognosis |
Directions to Hospitals Treating Autoimmune polyendocrine syndrome |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Natural History
Prognosis
Type I: The prognosis of autoimmune polyendocrine syndrome type I is variable, depending on how organs are affected and the severity of the disease.
Type II: Prognosis of autoimmune polyendocrine syndrome type II depends on whether endocrine end-organ failures occur or not.
Type III: Prognosis of autoimmune polyendocrine syndrome type III depends on whether glandular failures occur or not.