Clinical characteristics of behçet’s disease in palestine, a retrospective cohort study
Abdalrahim Daraghma, Lamar Baidoun, Samaa Nazzal, Moath Hattab, Basil Jalamneh, Mahdi Abusalameh, Refat Hanbali, Qusay Abdoh

TL;DR
This study describes the clinical features and complications of Behçet’s Disease in Palestine, highlighting common symptoms and outcomes.
Contribution
The study provides the first detailed clinical characterization of Behçet’s Disease in Palestine.
Findings
Oral and genital ulcers were the most common initial symptoms in Palestinian BD patients.
Vascular events and visual impairment were the most frequent complications observed.
Neurological and neuropsychiatric complications were less common and showed no gender differences.
Abstract
Behçet’s Disease (BD) is a chronic, systemic vasculitis of unknown etiology that affects multiple organ systems. It is characterized by recurrent oral and genital ulcers, ocular involvement, affecting arteries and veins of all sizes. It is more prevalent in countries along the ancient Silk Road. Diagnosis is primarily clinical, as there are no specific laboratory tests. The International Criteria for BD (ICBD) was developed to improve diagnostic accuracy. Management requires a multidisciplinary approach, with treatment strategies depending on disease severity. Despite BD’s significant morbidity and diverse clinical manifestations, its prevalence and characteristics remain to be described in Palestine. This research provides critical insights into disease patterns and contributes to improved diagnosis and management in Palestine. A retrospective cohort study was conducted in the period…
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Taxonomy
TopicsOcular Diseases and Behçet’s Syndrome · Vasculitis and related conditions · Retinal and Optic Conditions
