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.

journal_name

Am J Ophthalmol

authors

Schuman JS,Lieberman KV,Friedman AH,Berger M,Schoeneman MJ

doi

10.1016/s0002-9394(14)73374-4

subject

Has Abstract

pub_date

1985-12-15 00:00:00

pages

822-7

issue

6

eissn

0002-9394

issn

1879-1891

pii

S0002-9394(14)73374-4

journal_volume

100

pub_type

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