The factors precipitating central nervous system (CNS) demyelination, including optic neuritis, remain largely unknown but are likely to represent a complex interplay between the patient's environment and their genetic background. We report the development of sequential demyelinating optic neuritis in a patient with genetically confirmed Charcot-Marie-Tooth disease type 1A, a hereditary neuropathy. This neuropathy is characterized by duplication of peripheral myelin protein 22 (PMP22), which results in structurally abnormal peripheral myelin.
View Article and Find Full Text PDFPurpose: To evaluate differences in visual recovery after phacoemulsification with direct or tilted surgical microscope illumination using a macular photostress test.
Setting: Western Eye Hospital, Imperial College Health Care National Health Service Trust, London, United Kingdom.
Methods: This randomized double-masked controlled trial enrolled patients presenting to a daycare unit for single-eye cataract surgery.