Falciform fold, retinal detachment, and Norrie's disease.

Abstract:

:A patient with X-chromosome-linked recessive Norrie's disease, characterized by retinal falciform fold, retinal detachment, repeated vitreous hemorrhage, and retrolental membrane formation, was observed from age 6 weeks. The patient showed the clinical progression from these early retinal and vitreous changes to the more typical retrolental vascularized detached retina. Pathologic examination showed normal retinal tissue. Two other male relatives showed the end stages of Norrie's disease with bilateral congenital blindness, with and without mental retardation and deafness. Vitreoretinal surgery prevented phthisis bulbi from occurring the operated eye but was unsuccessful in reattaching the contracted retina.

journal_name

Am J Ophthalmol

authors

Jacklin HN

doi

10.1016/s0002-9394(14)75079-2

subject

Has Abstract

pub_date

1980-07-01 00:00:00

pages

76-80

issue

1

eissn

0002-9394

issn

1879-1891

pii

S0002-9394(14)75079-2

journal_volume

90

pub_type

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