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

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

doi:10.1016/S0002-9394(14)73374-4

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

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

Biomedical Engineering

Research output: Contribution to journal › Article › peer-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 language	English (US)
Pages (from-to)	822-827
Number of pages	6
Journal	American Journal of Ophthalmology
Volume	100
Issue number	6
DOIs	https://doi.org/10.1016/S0002-9394(14)73374-4
State	Published - 1985

ASJC Scopus subject areas

Ophthalmology

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10.1016/S0002-9394(14)73374-4

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title = "Senior-Loken syndrome (familial renal-retinal dystrophy) and Coats' disease",

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.",

author = "Schuman, {J. S.} and Lieberman, {K. V.} and Friedman, {A. H.} and M. Berger and Schoeneman, {M. J.}",

note = "Funding Information: From the Departments of Ophthalmology (Drs. Schuman and Friedman) and Pediatrics (Drs. Lieberman, Berger, and Schoeneman), Mount Sinai School of Medicine, New York, New York. This study was supported in part by an unrestricted grant from Research to Prevent Blindness, Inc., New York, New York.",

year = "1985",

doi = "10.1016/S0002-9394(14)73374-4",

language = "English (US)",

volume = "100",

pages = "822--827",

journal = "American Journal of Ophthalmology",

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T1 - Senior-Loken syndrome (familial renal-retinal dystrophy) and Coats' disease

AU - Schuman, J. S.

AU - Lieberman, K. V.

AU - Friedman, A. H.

AU - Berger, M.

AU - Schoeneman, M. J.

N1 - Funding Information: From the Departments of Ophthalmology (Drs. Schuman and Friedman) and Pediatrics (Drs. Lieberman, Berger, and Schoeneman), Mount Sinai School of Medicine, New York, New York. This study was supported in part by an unrestricted grant from Research to Prevent Blindness, Inc., New York, New York.

PY - 1985

Y1 - 1985

N2 - 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.

AB - 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.

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

Abstract

ASJC Scopus subject areas

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