Results 51 to 60 of about 101,671 (163)
HLA-B51 gene and its expression in association with Behçet's Disease in Denizli Province of Turkey
Behçet's Disease (BD) is a multisystemic inflammatory disorder as a triad of symptoms including recurrent oral and genital aphthous ulceration, and uveitis with unknown pathogenesis.
Tatlıpınar, Sinan +6 more
core +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
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
Human leukocyte antigen-associated uveitis in Thai population: Brief review
Human Leukocyte Antigen (HLA) has been associated with several immune-mediated diseases, malignancies and infectious diseases. Due to the HLA complexity and polymorphisms, several types of HLA have been used as the molecular markers in diagnosis.
Nampeung Anukul +2 more
doaj
Behçet’s Disease and Tuberculosis: A Complex Relationship
Behçet’s disease (BD) is a systemic vasculitis characterized by recurrent orogenital ulceration and several systemic manifestations (such as gastrointestinal involvement, vascular disease or arthritis).
Sara Mendonça Freitas +4 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
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
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
doaj
The high prevalence of nasopharyngeal cancer (NPC) in Southern Asia and Mediterranean Northern Africa suggests genetic predisposition among other factors.
Stroncek David +13 more
doaj +1 more source

