Autoimmune polyglandular syndrome type 2
Other Names for this Disease
- Autoimmune polyendocrine syndrome type 2
- Diabetes mellitus, Addison's disease, myxedema
- Multiple endocrine deficiency syndrome, type 2
- PGA 2
autoimmune disorder that affects many hormone-producing (endocrine) glands. This condition is characterized by the presence of Addison's disease along with autoimmune thyroid disease and/or type 1 diabetes. Affected individuals may also have problems with other endocrine glands. Autoimmune polyglandular syndrome type 2 is diagnosed in adulthood, typically around age 30. This condition occurs more often in women than men, and treatment primarily involves hormone replacement therapy. The cause of autoimmune polyglandular syndrome type 2 is unknown, although it may involve a combination of genetic and environmental factors.Autoimmune polyglandular syndrome type 2 is an
Last updated: 3/24/2010
- Sivarajah S, Fan CY, Akinsoto OPA. Polyglandular Autoimmune Syndrome, Type II. eMedicine Journal. October 2, 2008; http://emedicine.medscape.com/article/124287-overview. Accessed 3/24/2010.
- Polyglandular Deficiency Syndromes. Merck Manual for Healthcare Professionals. November 2009; http://www.merck.com/mmpe/sec12/ch154/ch154a.html. Accessed 3/24/2010.
- The Merck Manuals Online Medical Library provides information on this condition for patients and caregivers.
- The National Endocrine and Metabolic Diseases Information Service, a service of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), provides information on this topic. Click on the link to view the information on this topic.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
- Medscape Reference provides information on this topic. Click on the link to view this information. You may need to register to view the medical textbook, but registration is free.
- The Online Mendelian Inheritance in Man (OMIM) is an catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Autoimmune polyglandular syndrome type 2. Click on the link to view a sample search on this topic.