Srujay Pandiri, Celine Chaaya, Ryan S Meshkin, Sandra Hoyek, Joseph F Rizzo, Diana Tambala, Emily Da Cruz, Anna Lynch, Ryan Gise, Patricia L Musolino, Nimesh A Patel
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Ophthalmic Artery Occlusion as a Novel Ophthalmic Manifestation of ACTA2- Related Vascular Smooth Muscle Disorder.
This case describes a 12-year-old patient with a known history of an actin-alpha 2 (ACTA2) gene mutation who presented with an ophthalmic artery occlusion (OAO). The patient's medical history was significant for multiple strokes and a left homonymous hemianopia. She presented to the emergency department with acute visual loss in the right eye and hypertension and was diagnosed with an OAO affecting the right eye. The aim of this report is to highlight a unique ophthalmic complication associated with ACTA2 mutations not previously documented in the literature.
期刊介绍:
OSLI Retina focuses exclusively on retinal diseases, surgery and pharmacotherapy. OSLI Retina will offer an expedited submission to publication effort of peer-reviewed clinical science and case report articles. The front of the journal offers practical clinical and practice management features and columns specific to retina specialists. In sum, readers will find important peer-reviewed retina articles and the latest findings in techniques and science, as well as informative business and practice management features in one journal.