Biochemical and Histological Analysis of 'Recurrent' Macular Corneal Dystrophy
- 1 July 1982
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 100 (7) , 1125-1131
- https://doi.org/10.1001/archopht.1982.01030040103019
Abstract
• A patient with macular corneal dystrophy who had a successful 6-mm corneal transplant 23 years ago underwent a second keratoplasty for marked irregular astigmatism. The excised button, which contained the original graft and a rim of host cornea, was divided into several portions. One portion was examined histologically, another portion was incubated in organ culture with radioactive precursors and the biosynthetically labeled products characterized, and a third portion was used for cell culture and karotype analysis. The results indicated that host stromacytes had not invaded the graft and that graft stromacytes had synthesized normal proteoglycans. Furthermore, although there was excessive synthesis of abnormal proteoglycan by host stromacytes and accumulation of this material in the host cornea, minor amounts of this material actually accumulated in the graft cornea, possibly contributing to the astigmatism. A large transpant that would leave a minimum of host corneal tissue may be conducive to a longer-term good result in patients with macular corneal dystrophy.This publication has 6 references indexed in Scilit:
- DETECTION OF SPECIFIC COLLAGEN TYPES IN NORMAL AND KERATOCONUS CORNEAS1981
- Macular corneal dystrophy: failure to synthesize a mature keratan sulfate proteoglycan.Proceedings of the National Academy of Sciences, 1980
- Characterization and biosynthesis of proteoglycans of corneal stroma from rhesus monkey.Journal of Biological Chemistry, 1979
- MACULAR CORNEAL-DYSTROPHY - STUDIES OF SULFATED GLYCOSAMINOGLYCANS IN CORNEAL EXPLANT AND CONFLUENT STROMAL CELL-CULTURES1977
- Recurrence of Hereditary Corneal Dystrophy Following KeratoplastyAmerican Journal of Ophthalmology, 1973
- MACULAR CORNEAL DYSTROPHY - INHERITED ACID MUCOPOLYSACCHARIDE STORAGE DISEASE OF CORNEAL FIBROBLAST1964