Managing intraocular inflammation requires precision and multidisciplinary coordination. Uveitis and ocular inflammation represent complex disorders that may arise from autoimmune diseases, infections, or systemic conditions. Accurate classification—whether anterior, intermediate, posterior, or pan-uveitis—guides the therapeutic pathway. The increasing use of imaging modalities like fluorescein angiography and OCT has significantly improved diagnostic precision, especially in detecting subclinical inflammation. Biologic agents and steroid-sparing immunomodulatory therapies now offer targeted relief while minimizing systemic side effects. Collaboration with rheumatologists and infectious disease specialists ensures underlying causes are addressed effectively. Advances in sustained-release drug delivery systems, including injectable implants, are extending control over chronic inflammation. Early intervention remains key to preserving vision, as chronic uveitis can lead to complications like glaucoma or macular edema if left untreated.
Title : Rare and interesting case of Goldenhar’s syndrome in a 3 years old male child
Gowhar Ahmad, Florence Hospital Srinagar, India
Title : Diagnostic uncertainty with a patient presenting with raised intra-ocular pressure. A unique case of choroidal melanoma
Raheel Faiz, UHCW, United Kingdom
Title : Subthreshold micropulse laser for residual subretinal fluid after vitrectomy in myopic tractional maculopathy?A randomized controlled trial
Zhang Xifang, Beijing Tongren Hospital, China
Title : Hitting the trifecta-ocular syphilis
Lisa Sunny, Aravind Eye Hospital, India
Title : Lumevoq gene therapy in leber hereditary optic neuropathy
Magali Taiel, GenSight Biologics, France
Title : The effect of low hypermetropia correction and office-based orthoptic training on binocular vision parameters in children with convergence insufficiency
Agnieszka Rosa, Orticus Center for the Treatment of Strabismus and vision Disorders, Poland