TY  - CHAP
M1  - Book, Section
TI  - Chapter 166. Adamantiades–Behçet Disease
A1  - Zouboulis, Christos C.
A2  - Goldsmith, Lowell A.
A2  - Katz, Stephen I.
A2  - Gilchrest, Barbara A.
A2  - Paller, Amy S.
A2  - Leffell, David J.
A2  - Wolff, Klaus
PY  - 2012
T2  - Fitzpatrick's Dermatology in General Medicine, 8e
AB  - |PrintAdamantiades–Behçet  Disease  at  a  GlanceRare  disease  with  worldwide  distribution  but  strongly  varying  prevalence;  certain  ethnic  groups  are  mainly  affected.A  genetically  determined  disorder  with  a  probable  environmental  triggering  factor.Multisystem  occurrence,  with  oral  aphthous  ulcers,  genital  ulcers,  papulopustules,  erythema  nodosum-like  lesions,  uveitis,  and  arthropathy  as  most  common  signs.Inflammatory  disease  representing  a  neutrophilic  vascular  reaction  or  vasculitis.Chronic  relapsing  progressive  course  and  potentially  poor  prognosis  (especially  in  males  with  systemic  presenting  signs;  mortality,  0–6%).  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessmedicine.mhmedical.com/content.aspx?aid=56079113
ER  -