doiSerbia

Morning glory syndrome associated with primary open angle glaucoma: Case report

Božić Marija (Faculty of Medicine, Belgrade + Clinic for Eye Diseases, Clinical Center of Serbia, Belgrade)
Hentova-Senćanić Paraskeva (Faculty of Medicine, Belgrade + Clinic for Eye Diseases, Clinical Center of Serbia, Belgrade)
Marković Vujica (Faculty of Medicine, Belgrade + Clinic for Eye Diseases, Clinical Center of Serbia, Belgrade)
Marjanović Ivan (Clinic for Eye Diseases, Clinical Center of Serbia, Belgrade)

Introduction. Morning glory syndrome (MGS) is a rare congenital optic disc anomaly, first reported in 1970. MGS is a nonprogressive and untreatable condition, which usually occurs as an isolated ocular anomaly, and can be associated with the increased incidence of nonrhegmatogenous retinal detachment, and also with strabismus, afferent pupillary defect, visual field defects, presence of hyaloids artery remnants, ciliary body cyst, congenital cataract, lid hemangioma and preretinal gliosis. Case Outline. We report a clinical case of MGS associated with primary open angle glaucoma. The use of sophisticated diagnostic tools, such as retinal tomography and visual field testing is limited if multiple eye conditions are present, since optic disc does not have “usual” appearance that can be analyzed according to standard statistical databases. Conclusion. In treating and follow up of glaucoma cases associated with other diseases and conditions that affect the appearance and function of the optic nerve head, sometimes the use of modern technological methods is limited due to difficult interpretation of the obtained results.

Keywords: glaucoma, morning glory, syndrome