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小儿年龄组眼部及其附属器先天性缺陷的谱系;尼日利亚一家三级医疗机构的经验。

Spectrum of congenital defects of the eye and its adnexia in the pediatric age group; experience at a tertiary facility in Nigeria.

作者信息

Adekoya Bola J, Balogun Modupe M, Balogun Bola G, Ngwu Rosemary A

机构信息

Department of Ophthalmology, Lagos State University Teaching Hospital (LASUTH), P.O. Box 19484, Ikeja, 100001, Lagos, Nigeria,

出版信息

Int Ophthalmol. 2015 Jun;35(3):311-7. doi: 10.1007/s10792-014-9946-4. Epub 2014 Apr 18.

Abstract

The aim of this study was to investigate the types and presentation pattern of congenital defects of the eye and adnexia in our center. This is a retrospective review of congenital defects of the eye and adnexia over a 20-month period at a tertiary referral center in Lagos, Nigeria. Records were analyzed for age at presentation, laterality, gender, vision assessment, and type(s) of abnormality. Out of 412 pediatric patients, 40 (9.7 %) were seen to have congenital abnormality of the eye and/or its adnexia during the study period. There were 17 (42.5 %) males. Twelve patients (30.0 %) presented with involvement of the right eyes, nine (22.5 %) with left eyes, while 19 (47.5 %) had bilateral involvement. Twenty-eight patients (70.0 %) were aged 1 year or less at the time of presentation. A total of 69 entities were recognized as some children had two or more malformations. The common congenital defects identified were cataract (39.1 %), ptosis (17.4 %), glaucoma (8.7 %), and cornea opacity (7.2 %). Other less common congenital defects include: microphthalmos, anophthalmos, coloboma (lid and iris), dermoid cyst, and aniridia. All of the patients with available visual acuity documentation had visual impairment. A high proportion of the patients were lost to follow-up. Cataract, ptosis, and glaucoma were the commonest congenital defects of the eye and adnexia in our center and were associated with visual impairments. The significant loss of the patients during follow-up needs urgent investigation and attention to forestall this trend.

摘要

本研究的目的是调查我院中心眼部及附属器先天性缺陷的类型和表现模式。这是一项对尼日利亚拉各斯一家三级转诊中心20个月期间眼部及附属器先天性缺陷的回顾性研究。分析了患者的就诊年龄、病变侧别、性别、视力评估及异常类型。在412例儿科患者中,40例(9.7%)在研究期间被发现有眼部和/或其附属器的先天性异常。其中男性17例(42.5%)。12例患者(30.0%)右眼受累,9例(22.5%)左眼受累,19例(47.5%)双眼受累。28例患者(70.0%)就诊时年龄在1岁及以下。共识别出69种病变情况,因为有些儿童有两种或更多畸形。所发现的常见先天性缺陷为白内障(39.1%)、上睑下垂(17.4%)、青光眼(8.7%)和角膜混浊(7.2%)。其他不太常见的先天性缺陷包括:小眼球、无眼球、睑裂和虹膜缺损、皮样囊肿及无虹膜。所有有视力记录的患者均有视力损害。很大一部分患者失访。白内障、上睑下垂和青光眼是我院中心眼部及附属器最常见的先天性缺陷,且与视力损害相关。患者在随访期间大量失访的情况需要紧急调查并予以关注,以阻止这种趋势。

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