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.

作者信息

Saffra Norman A, Emborgo Trisha S, Laureta Emma C, Kirsch David S, Guarini Ludovico

机构信息

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.

出版信息

J Neuroophthalmol. 2022 Mar 1;42(1):e367-e370. doi: 10.1097/WNO.0000000000001233. Epub 2021 Apr 14.

DOI:10.1097/WNO.0000000000001233

PMID:33870946

Abstract

摘要

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