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dc.contributor.authorYazici, H.
dc.contributor.authorEsen, F.
dc.date.accessioned2021-03-05T08:03:21Z
dc.date.available2021-03-05T08:03:21Z
dc.date.issued2008
dc.identifier.citationYazici H., Esen F., "Mortality in Behcet's syndrome", CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.26, 2008
dc.identifier.issn0392-856X
dc.identifier.othervv_1032021
dc.identifier.otherav_96f536db-55c6-4c76-a9db-3ce37ddbe515
dc.identifier.urihttp://hdl.handle.net/20.500.12627/101609
dc.description.abstractBehcet's syndrome significantly increases mortality especially when seen in the young male, while it is less severe among females and the aged. In many patients, the condition abates with the passage of time. The main cause of mortality is large vessel disease, especially bleeding pulmonary artery aneurysms (PAA), almost exclusively seen among men. Central nervous system disease comes second. Interestingly, not much increased atherosclerosis is seen in Behcet's syndrome when compared to other inflammatory diseases. In controlled studies, there has been no increase in history of increased angina or myocardial infarction. Similarly, atherosclerosis plaque formation is not increased by ultrasound. On the other hand, intermittent caludication can be seen. However, this is not due to arterial involvement but due to venous disease of the lower extremities. Recentl;y there has been a substantial decrease in mortality due to PAA thanks to prompt disease recognition and treatment.
dc.language.isoeng
dc.subjectTıp
dc.subjectROMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.titleMortality in Behcet's syndrome
dc.typeMakale
dc.relation.journalCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume26
dc.identifier.issue5
dc.contributor.firstauthorID189289


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