Comprehensive Clinical Overview of Grayson–Wilbrandt Corneal Dystrophy (GWCD): A Rare Autosomal Recessive Mitochondrial Disorder

1. Nomenclature & Classification Grayson–Wilbrandt Corneal Dystrophy (GWCD; OMIM #618546), often informally referred to as “Grayson’s Syndrome,” is a very rare, autosomal recessive corneal dystrophy classified under the mitochondrial subtype…

Continue ReadingComprehensive Clinical Overview of Grayson–Wilbrandt Corneal Dystrophy (GWCD): A Rare Autosomal Recessive Mitochondrial Disorder