Abstract |
A case history of a newborn infant is discussed. At birth he showed bilateral buphthalmos with aniridia and congenital corneal opacities, agreeing with Peters' anomaly. A keratoplasty was performed. The dysgenesis mesenchymalis classification is mentioned briefly. High resolution banding technique of chromosomes revealed no abnormality.
|
Authors | R Koster, A T van Balen |
Journal | Ophthalmic paediatrics and genetics
(Ophthalmic Paediatr Genet)
Vol. 6
Issue 1-2
Pg. 241-6
(Aug 1985)
ISSN: 0167-6784 [Print] Netherlands |
PMID | 3934622
(Publication Type: Case Reports, Journal Article)
|
Topics |
- Cornea
(pathology)
- Corneal Opacity
(complications, congenital, embryology, genetics, pathology)
- Eye Abnormalities
- Humans
- Iris
(abnormalities)
- Karyotyping
- Male
|