Nondetectable cone and rod electroretinographic responses in a patient with Cockayne syndrome.
Jpn J Ophthalmol
; 39(4): 420-3, 1995.
Article
en En
| MEDLINE
| ID: mdl-8926650
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.
Buscar en Google
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Síndrome de Cockayne
/
Células Fotorreceptoras Retinianas Conos
Límite:
Child
/
Female
/
Humans
Idioma:
En
Revista:
Jpn J Ophthalmol
Año:
1995
Tipo del documento:
Article
País de afiliación:
Japón