Senior-Loken syndrome (familial renal-retinal dystrophy) and Coats' disease

J. S. Schuman, K. V. Lieberman, A. H. Friedman, M. Berger, M. J. Schoeneman

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Senior-Loken syndrome is a rare hereditary disease that combines a disorder resembling familial juvenile nephronophthisis with retinitis pigmentosa. Retinitis pigmentosa is even less frequently associated with exudative retinopathy. The patient, a 15-year-old boy, had hereditary renal-retinal dystrophy combined with an exudative vasculopathy of the Coats' type. The patient is on thrice-weekly hemodialysis after two kidney transplants failed. One eye became painful and blind and was eventually enucleated.

    Original languageEnglish (US)
    Pages (from-to)822-827
    Number of pages6
    JournalAmerican Journal of Ophthalmology
    Volume100
    Issue number6
    DOIs
    StatePublished - 1985

    ASJC Scopus subject areas

    • Ophthalmology

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