Results 41 to 50 of about 2,566 (126)
Epidemiology of human leukocyte antigens among omani population
Oman is located on the Southeastern coast of the Arabian Peninsula, and its population has high levels of consanguinity. Human leukocytic antigen (HLA) typing analysis in human population holds unexploited potential for elucidating the genetic causes of ...
Issa Al Salmi +6 more
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We report a case of recurrent oral/scrotal ulcers with systemic symptoms in a 33‐year‐old man masked pulmonary tuberculosis: imaging showed cavitary consolidations with effusion, and thoracoscopic pleural biopsy demonstrated acid‐fast bacilli. Anti‐tubercular therapy led to complete resolution, underscoring TB as a key Behçet's mimic to exclude before ...
Rinoosha Rachel +4 more
wiley +1 more source
Coexistence of Behçet's Disease and Ankylosing Spondylitis
Whether Behçet's disease (BD) is of the seronegative spondyloarthropathy (SSpA) group has been a subject of debate for many years.[] Behçet's syndrome is now not considered to belong to the SSpA group[] but is considered to be a systemic vasculitis ...
Canan ÇELİK +3 more
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Interdisciplinary Approaches to Diagnostic Analysis in Behcet’s Disease
The exploration of Behçet’s disease challenges the idea that “the oral cavity reflects systemic diseases.” This chronic systemic vasculitis, characterized by oral and genital ulcers, cutaneous lesions, and multi-organ involvement, poses diagnostic ...
Arun Dev Sharma +3 more
doaj +1 more source
Purpose: To report a unique case of Behçet's disease that presented with atypical ocular manifestations. Methods: Case report. Results: A 23-year-old homosexual male presented with bilateral anterior uveitis, vitritis, neuroretinitis and a unilateral ...
Roy Schwartz +6 more
doaj +1 more source
Journal of Paediatrics and Child Health, Volume 62, Issue 6, Page 1060-1065, June 2026.
Briana Davis +3 more
wiley +1 more source
Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report
Kikuchi–Fujimoto Disease (KFD) is a rare, typically self‐limiting inflammatory condition primarily associated with fever, cervical lymphadenopathy, and occasionally small‐vessel vasculitis. Central nervous system (CNS) involvement in KFD is exceedingly rare and has been described in isolated cases, including encephalitis, aseptic meningitis, and ...
Yusuf Kagzi +5 more
wiley +1 more source
Clinical case report: Behcet’s Uveitis: Diagnostic Challenges and Modern Treatment Approach
The article analyzes the clinical observation of a 22-year-old patient with severe recurrent bilateral uveitis complicated by neuroretinitis, probably caused by Behcet’s disease.
D. S. Atarshchikov +4 more
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Behçet's disease: Clinical and demographic associations
AIM: To comparatively study the clinical manifestations, sexual and HLA-B51 associations in patients with Behçet's disease (BD) in two ethnic groups/MATERIAL AND METHODS: The authors examined 143 patients with the valid diagnosis of BD who were divided ...
Z S Alekberova +2 more
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Pediatric Behçet’s disease: Experience of a single tertiary center
Objectives: The aim of this study was to examine the clinical and phenotypic features of pediatric Behçet’s disease (PEDBD) in our clinic and present the rates of fulfilling the diagnostic criteria.
Ceyhun Açarı +4 more
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