Nondetectable cone and rod electroretinographic responses in a patient with Cockayne syndrome.

Abstract:

:A 10-year-old girl complained or poor vision in both eyes. The patient showed progeria, physical and mental retardation, sensorineural hearing loss, cutaneous photosensitivity, hyperopia, poor pupillary dilation, exotropia, salt-and-pepper fundi, nondetectable cone and rod electroretinographic (ERG) responses, cerebral atrophy on computed tomography, and demyelination of periventricular white matter on magnetic resonance imaging. We believe that nondetectable cone and rod ERG responses in Cockayne syndrome, as demonstrated in our patient, may be uncommon.

journal_name

Jpn J Ophthalmol

authors

Ikeda N,Yamamoto S,Hayasaka S,Fukuo Y,Koike T

subject

Has Abstract

pub_date

1995-01-01 00:00:00

pages

420-3

issue

4

eissn

0021-5155

issn

1613-2246

journal_volume

39

pub_type

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