Congenital Aniridia
Journal of the Korean Ophthalmological Society
; : 535-539, 1995.
Article
in Korean
| WPRIM (Western Pacific)
| ID: wpr-63446
Responsible library:
WPRO
ABSTRACT
Aniridia is a very rare disorder the main features of which are congenitally partial or nearly complete absence of the iris and foveal hypoplasia. The authors obseved aniridia in two generations, mother and one daughter. They have cataract, ectopia lentis, nystagmus and foveal hypoplasia as well as aniridia. The lens of daughter was aspirated in both eyes consecutively. Her final best corrected visual acuity was 0.3 with +sph. 13.00D in each eyes.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Cataract
/
Nuclear Family
/
Visual Acuity
/
Aniridia
/
Ectopia Lentis
/
Family Characteristics
/
Iris
/
Mothers
Limits:
Humans
Language:
Korean
Journal:
Journal of the Korean Ophthalmological Society
Year:
1995
Document type:
Article