Ectodermal Dysplasia with Bilateral Punctal Agenesis in a Nigerian Child: A Case Report

J. Owoeye, K. Monsudi, I. Yusuf, O. Bamidele
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Abstract

Ectodermal dysplasia (ED) is a hereditary condition that occurs worldwide. It is due to abnormality in the development of skin and its appendages (hair, teeth and nail). ED also presents with ocular manifestations. This case of ED is reported to highlight ocular manifestations such as bilateral punctal agenesis, madarosis and blepharitis. The need for a multi-disciplinary approach in managing such cases is underscored.
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尼日利亚儿童外胚层发育不良伴双侧点状发育不全1例
外胚层发育不良(ED)是一种发生在世界各地的遗传性疾病。这是由于皮肤及其附属物(头发、牙齿和指甲)发育异常引起的。ED也有眼部表现。据报道,ED的病例突出了眼部表现,如双侧泪点发育不全、madarosis和睑缘炎。强调需要采用多学科方法来处理此类案件。
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0.10
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审稿时长
20 weeks
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