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Congenital corneal opacity (Peters' anomaly) combined with buphthalmos and aniridia.

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.
AuthorsR Koster, A T van Balen
JournalOphthalmic paediatrics and genetics (Ophthalmic Paediatr Genet) Vol. 6 Issue 1-2 Pg. 241-6 (Aug 1985) ISSN: 0167-6784 [Print] NETHERLANDS
PMID3934622 (Publication Type: Case Reports, Journal Article)
Topics
  • Cornea (pathology)
  • Corneal Opacity (complications, congenital, embryology, genetics, pathology)
  • Eye Abnormalities
  • Humans
  • Iris (abnormalities)
  • Karyotyping
  • Male

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