Juvenile Behçet's disease: a tertiary center experience.
Zahide Ekinci TekinElif ÇelikelFatma AydınTuba KurtMüge SezerPakize Nilüfer TekgözCüneyt KaragölSerkan CoşkunMelike Mehveş KaplanBanu Çelikel AcarPublished in: Clinical rheumatology (2021)
In this cohort, the prevalence of genital ulceration and family history was high, and we observed less ocular involvement, a few permanent neurological morbidities and no death. Key Points • In the present study, there were acceptable permanent neurological involvements as morbidity and no mortality. • It is important noticing and managing jBD in early phase in order to prevent the devastating results. • The awareness of jBD provides timely treatment of patients. • The positivity of family history and HLA B51 should alert the clinician about the incomplete cases.