Behcet Disease: Sensitivity and Specificity
Introduction: The following is a review article from 2009:
Behçet's disease--a contemporary review.
Mendes D, Correia M, Barbedo M, Vaio T, Mota M, Gonçalves O, Valente J.
J Autoimmun. 2009 May-Jun;32(3-4):178-88. Epub 2009 Mar 26.
Behcet disease is a systemic inflammatory vasculitis of unknown etiology, though likely autoimmune in nature.
Areas of involvement include:
Oral ulcers
Genital ulcers
Ocular disease
Cutaneous lesions
Neurologic disease
Vascular disease
Cardiac disease
Gatrointestinal disease
Articular involvement
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Prevalence
Population / Calculator | Prevalence | Comments / Study / Link |
Turkish Population | 0.08% | In Turkish population betwen 80 - 420 per 100,000
Behçet's disease--a contemporary review. Mendes D, Correia M, Barbedo M, Vaio T, Mota M, Gonçalves O, Valente J. J Autoimmun. 2009 May-Jun;32(3-4):178-88. Epub 2009 Mar 26. |
Japanese Population | 0.007% | 7 - 8.5 in 10,000 in Japan
Behçet's disease--a contemporary review. Mendes D, Correia M, Barbedo M, Vaio T, Mota M, Gonçalves O, Valente J. J Autoimmun. 2009 May-Jun;32(3-4):178-88. Epub 2009 Mar 26. |
Norther Europe and United States | 0% | 0.12 to 0.64 per 100,000 in Northen Europe and United States
Behçet's disease--a contemporary review. J Autoimmun. 2009 May-Jun;32(3-4):178-88. Epub 2009 Mar 26. Mendes D, Correia M, Barbedo M, Vaio T, Mota M, Gonçalves O, Valente J. PMID
19324519 |
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The sensitivity and specificity of findings for Behcet Disease are listed below. See the left navigation bar to change the display.