Asymptomatic Retinal Vein Occlusion in a 13-Year-Old With Heterozygous Deletion of the PMP22 Gene and a Diagnosis of Hereditary Neuropathy With Liability to Pressure Palsies.

Autor: Saffra NA; Department of Ophthalmology (NAS), Maimonides Medical Center, Brooklyn, New York; Department of Ophthalmology (NAS, TSE, DSK), St. John's Episcopal Hospital, Far Rockaway, New York; Department of Pediatric Neurology (ECL), Northwell Health, New Hyde Park, New York; and Division of Pediatric Hematology/Oncology (LG), Maimonides Children Hospital, Maimonides Medical Center, Brooklyn, New York., Emborgo TS, Laureta EC, Kirsch DS, Guarini L

Publikováno v: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society [J Neuroophthalmol] 2022 Mar 01; Vol. 42 (1), pp. e367-e370. Date of Electronic Publication: 2021 Apr 14.