المقالات العلمية

Normal electro-oculography in a young Omani male with genetically confirmed best disease complicated by choroidal neovascularization

… y heterozygous mutations in the bestrophin1 gene. Patients with this condition typically have an abnormal electrooculogram. We report a case of a 16-year-old male who presented with gradual progressive vision loss in the right eye. Ophthalmic assessment included funduscopy, optical coherence tomography (OCT), fluoresce …