A Case Report of Bilateral Congenital Ectropion in a Rare Collodion Baby
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© UPJO, 2023 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit https://creativecommons.org/licenses/by-nc-sa/4.0/.
Collodion baby syndrome also known as lamellar ichthyosis, is a rare genetic disorder with an incidence of 1 in 3 lacs live birth. It is characterized by tight shiny membrane covering the body like a plastic wrap.1 On shedding of membrane dry rough scaly skin like that of fish is visible. The ocular feature typical of this syndrome is ectropion which is mainly bilateral, however cases with unilateral ectropion have also been reported.2 The ectropion present in these children makes them prone to exposure keratopathy which could be sight threatening. It is a rare clinical condition in which timely intervention and conservative management can prevent permanent vision loss because of exposure to keratopathy.3-5 So, we are reporting a rare case of bilateral congenital ectropion.Abstract
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