1. A rare case of bilateral congenital corneal malformations
- Author
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J. Becker, Sabine Salla, Claudia Redbrake, and M. Reim
- Subjects
medicine.medical_specialty ,Blepharoplasty ,genetic structures ,medicine.medical_treatment ,Surgical Flaps ,Cornea ,Corneal Opacity ,Ophthalmology ,Rare case ,medicine ,Humans ,Sclerocornea ,Child ,business.industry ,Eyelids ,Staphyloma ,General Medicine ,medicine.disease ,eye diseases ,Scleral Diseases ,Surgery ,Left eye ,medicine.anatomical_structure ,Female ,Corneal staphyloma ,sense organs ,Perforating keratoplasty ,business ,Keratoplasty, Penetrating ,Follow-Up Studies - Abstract
We report the case of a now 6-year-old girl who was born with different abnormalities in each eye. The right eye showed a total sclerocornea. At the age of 4 years we performed a perforating keratoplasty. On the left eye a large staphyloma developed. The staphyloma was excised and a cornea with a scleral rim was fixed in. This transplant became cloudy under a conjunctival flap and blepharoplasty. In addition to the clinical follow-up, histological and immun-histochemical examinations of the corneas were carried out.
- Published
- 2009
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