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Multimodal imaging in a case of rubella retinopathy

  • Brian Lee
    Affiliations
    Doheny Eye Institute, Los Angeles, Calif

    Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, Calif.
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  • Giulia Corradetti
    Affiliations
    Doheny Eye Institute, Los Angeles, Calif

    Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, Calif.
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  • SriniVas R. Sadda
    Correspondence
    Correspondence to SriniVas R. Sadda, Doheny Eye Institute, Department of Ophthalmology, David Geffen School of Medicine at UCLA, 1355 San Pablo Street, Los Angeles, CA 90033
    Affiliations
    Doheny Eye Institute, Los Angeles, Calif

    Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, Calif.
    Search for articles by this author
Published:March 26, 2022DOI:https://doi.org/10.1016/j.jcjo.2022.02.024
      A 61-year-old female with congenital rubella and deafness presented for age-related macular degeneration. Ultrawide-field colour scanning laser ophthalmoscopy (A) revealed salt-and-pepper retinopathy with macular hypopigmentation and peripheral hyperpigmentation. On retroillumination (B), the hypopigmentation appeared hyperreflective, whereas the hyperpigmentation appeared hyporeflective. Both areas showed similar mottling on autofluorescence (C). Optical coherence tomography (D) showed focal areas of retinal pigment epithelium thickening centrally.
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