Marginal infiltrates arise from a wide variety of causes and according to the recent literature occur most commonly in association with chronic staphylococcal blepharitis. Marginal infiltrates often have a crescent form or coalesce to form a complete ring concentric to the limbus. On the other hand, the well-formed manifestation of an immunological process in the cornea, the so-called immunolog...

PURPOSE To describe a bilateral, central, oval corneal opacity not resembling any known corneal degeneration or dystrophy. METHODS Ophthalmic examination, corneal topography, and pachymetry. RESULTS A 30-year-old woman presented complaining of blurred vision. Biomicroscopic examination revealed bilateral, centrally located, oval, diffuse opacification of the anterior corneal stroma. Corneal...

PURPOSE To report the clinical results, postoperative progress, and complications after therapeutic keratoplasty for corneal perforation. METHODS Twenty consecutive eyes (20 patients) that underwent therapeutic keratoplasty between December 2003 and May 2006 were included. The eyes were evaluated retrospectively for the cause of the corneal perforation, the type of surgical technique and intr...

A subset of victims of ocular sulfur mustard (SM) exposure develops an irreversible, idiotypic keratitis with associated secondary pathologies, collectively referred to as mustard gas keratopathy (MGK). MGK involves a progressive corneal degeneration resulting in chronic ocular discomfort and impaired vision for which clinical interventions have typically had poor outcomes. Using a rabbit corne...

PURPOSE To clarify the usefulness of multilayer amniotic membrane transplantation in an unusual case of calcareous corneal degeneration in a patient with graft-versus-host disease. METHODS A 20-year-old Caucasian woman had bilateral calcareous corneal degeneration of one year of evolution, secondary to graft-versus-host disease. Treatment for both eyes with topical steroids and antibiotic oin...

Purpose Mutations in the gene encoding Gasdermin A3 (Gsdma3) have been described to cause severe skin phenotypes, including loss of sebaceous glands and alopecia, in mice. We discovered a novel C-terminal mutation in Gsdma3 in a new mouse line and characterized a less frequently reported corneal phenotype, likely caused by degeneration of Meibomian glands of the inner eyelid. Methods We used ...