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)...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Am J Ophthalmol Case Rep
Päätekijät: Seraly, Mark P., Badawi, Karim H., Gupta, Sumeet K., Jabbour, Nabil M., Ellis, Brian, Leys, Monique
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2020
Aiheet:
Case Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7595880/
https://ncbi.nlm.nih.gov/pubmed/33145458
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajoc.2020.100985
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