Author:
Malhotra Raman,Hernández-Martın Angela,Oji Vinzenz
Abstract
Congenital ichthyoses (CI) are rare genetic skin keratinisation diseases characterised by generalised scaling and a variable degree of erythema and hyperkeratosis. Ocular involvement includes the eyelids, conjunctiva and all layers of the cornea. Ophthalmic input should include regular slit lamp review with the primary aim to prevent a corneal epithelial defect, secondary bacterial infection, scarring or perforation. This review highlights the current literature regarding ophthalmic findings and management of CI.
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Cited by
14 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Inherited Disorders of Cornification;Rook's Textbook of Dermatology;2024-03-19
2. French national protocol for the management of congenital ichthyosis;Annales de Dermatologie et de Vénéréologie;2024-03
3. Advanced Anterior Eye Segment Imaging for Ichthyosis;Journal of Clinical Medicine;2023-09-16
4. Ichthyosis;Nature Reviews Disease Primers;2023-01-19
5. Scaly Skin, Bowed Bones, and Cloudy Cornea in a 7-Year-Old Child;Indian Journal of Paediatric Dermatology;2023