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Abstract Macular corneal dystrophy (MCD) is a rare congenital disease caused by mutations in the carbohydrate sulfotransferase 6 (chst6) gene. Patients suffer from opaque aggregates in the cornea leading to bilateral progressive vision loss by 4th decade of life. Corneal transplantation is the only available treatment, which is invasive, not available to every patient and recurrence of the symptoms is common.
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