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Rubella Retinopathy

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Abstract

The differential diagnosis of a “salt and pepper” fundus includes rubella retinopathy. Because most children with rubella have a constellation of other signs, it is easy to determine the diagnosis. These patients have deafness and cataracts that are present at birth or develop postnatally. The lenses show persistent nucleated epithelial cells in the cortex. Other ocular signs are glaucoma (due to incomplete angle cleavage) and microphthalmos. Systemically, these children may have abnormalities of the brain and heart. It is important that these lenses are removed carefully, as viruses are shed on extraction, which can produce an overwhelming uveitis. Phthisis bulbi may be the sequelae of an uneventful cataract procedure.

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Selected Reading

  • Collis WJ, Cohen DN (1970). Rubella retinopathy: a progressive disorder. Arch Ophthalmol 84: 33–35

    Article  PubMed  CAS  Google Scholar 

  • Wolff SM (1972). The ocular manifestations of congenital rubella. Trans Am Ophthalmol Soc 70: 577–580

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  • Yanoff M, Schaffer DB, Scheie HG (1968). Rubella ocular syndrome: clinical significance of viral and pathologic studies. Trans Am Acad Ophthalmol Otolaryngol 72: 89–92

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© 1993 Springer Science+Business Media New York

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Orellana, J., Friedman, A.H. (1993). Rubella Retinopathy. In: Clinico-Pathological Atlas of Congenital Fundus Disorders. Springer, New York, NY. https://doi.org/10.1007/978-1-4613-9320-7_9

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  • DOI: https://doi.org/10.1007/978-1-4613-9320-7_9

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4613-9322-1

  • Online ISBN: 978-1-4613-9320-7

  • eBook Packages: Springer Book Archive

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