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Autoimmune Polyglandular Syndrome, Type IIAka: Autoimmune Polyglandular Syndrome, APS II
- Epidemiology
- Prevalence: 2 per 100,000
- Age of Onset: 30-40 years
- Gender: Women affected 3 times more than men
- Risk Factors
- HLA haplotype DR3 (DQB*0201)
- HLA haplotype DR4 (DQB1*0302)
- Diagnosis
- Required Conditions for diagnosis
- Autoimmune Adrenal Insufficiency
- Presenting diagnosis in 50% of cases
- Associated with second autoimmune condition in 50%
- Autoimmune Thyroid disease
- Type I Diabetes Mellitus
- Commonly Associated Conditions (4-10%)
- Vitiligo
- Chronic atrophic Gastritis (and Pernicious Anemia)
- Hypergonadotropic Hypogonadism
- Chronic Autoimmune Hepatitis
- Alopecia
- Other Associated Conditions (<1%)
- Myasthenia Gravis
- Rheumatoid Arthritis
- Sjogren's Syndrome
- Presentation
- See Adrenal Insufficiency
- See other associated conditions listed above
- Diagnosis
- See Adrenal Insufficiency
- See other associated conditions listed above
- Management
- See Adrenal Insufficiency
- See other associated conditions listed above
- References
- Betterie (2002) Endocr Rev 23:327
- Majeroni (2007) Am Fam Physician 75(5):667
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