Suppr超能文献

患有缺指(趾)-外胚层发育不良-腭裂综合征家族中的角膜病变

Keratopathy in a family with the ectrodactyly-ectodermal dysplasia-clefting syndrome.

作者信息

Mawhorter L G, Ruttum M S, Koenig S B

出版信息

Ophthalmology. 1985 Oct;92(10):1427-31. doi: 10.1016/s0161-6420(85)33847-2.

Abstract

Four members of a family with the ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome and associated keratopathy are presented. The main features of this syndrome include lobster-claw deformities of the hands and feet, abnormalities of the hair and teeth, cleft lip and palate, nasolacrimal abnormalities, and a progressive keratopathy ranging in severity from an asymptomatic pannus to bilateral dense corneal scarring and neovascularization. Despite congenital limb abnormalities, the major functional disability of three of these patients stems from severe photophobia and decreased visual acuity secondary to the corneal disease. Treatment with cycloplegics, topical steroids, and bandage soft contact lenses was unsuccessful. The EEC syndrome is transmitted in an autosomal dominant manner. The spectrum of keratopathy demonstrated in this family can be explained by the different ages of the patients, by variation in gene penetrance and expressivity and by differing durations and severity of dacryocystitis and related keratoconjunctivitis. The etiology of the keratopathy appears to be primarily a manifestation of the underlying ectodermal dysplasia with probable contributions from associated tearfilm abnormalities and external ocular infection.

摘要

本文报告了一个患有缺指(趾)-外胚层发育不良-腭裂(EEC)综合征及相关角膜病变的家族中的四名成员。该综合征的主要特征包括手足呈龙虾爪样畸形、毛发和牙齿异常、唇腭裂、鼻泪管异常,以及一种进行性角膜病变,其严重程度从无症状的血管翳到双侧致密角膜瘢痕和新生血管形成不等。尽管存在先天性肢体异常,但其中三名患者的主要功能障碍源于严重畏光以及角膜疾病继发的视力下降。使用睫状肌麻痹剂、局部类固醇和绷带软性角膜接触镜治疗均未成功。EEC综合征以常染色体显性方式遗传。该家族中所显示的角膜病变谱可通过患者的不同年龄、基因外显率和表现度的差异以及泪囊炎和相关角结膜炎的不同病程和严重程度来解释。角膜病变的病因似乎主要是潜在外胚层发育不良的一种表现,可能还与相关的泪膜异常和眼外部感染有关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验