A rare case of occlusive juxtafoveolar retinal telangiectasias associated with lesions of the central nervous system: A cerebroretinal vasculopathy like phenotype without mutations in the TREX1 gene

A rare case of occlusive juxtafoveolar retinal telangiectasias associated with lesions of the central nervous system: A cerebroretinal vasculopathy like phenotype without mutations in the TREX1 gene

Purpose: To report a rare case of bilateral occlusive juxtafoveolar retinal telangiectasias associated with central nervous system lesions and renal impairment. Observations: A 47-year-old woman presented to clinic with subjective vision loss in the right eye with best-corrected visual acuity (BCVA)...

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Bibliographic Details
Main Authors: Mark P. Seraly, Karim H. Badawi, Sumeet K. Gupta, Nabil M. Jabbour, Brian Ellis, Monique Leys
Format: Article
Language:English
Published: Elsevier 2020-12-01
Series:American Journal of Ophthalmology Case Reports
Subjects:
Cerebroretinal vasculopathy
Occlusive retinal telangiectasis
Multimodal imaging
Optical coherence tomography angiography
TREX1
Online Access:http://www.sciencedirect.com/science/article/pii/S2451993620303005

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http://www.sciencedirect.com/science/article/pii/S2451993620303005

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