Suppr超能文献

先天性上睑下垂伴 VATER 综合征。

Congenital blepharoptosis co-occurring with VATER association.

机构信息

Department of Plastic Surgery, Kobe University, Graduate School of Medicine, Hyogo Prefectural Kobe Children's Hospital, Kobe, Japan.

出版信息

Ophthalmic Plast Reconstr Surg. 2010 Sep-Oct;26(5):374-6. doi: 10.1097/IOP.0b013e3181c9fdf0.

Abstract

VATER association is the tendency for 5 specific anomalies (vertebral and vascular anomalies [V], anal atresia [A], esophageal atresia and/or tracheoesophageal fistula [TE], and radial and renal anomalies [R]) to occur together in one individual. Recently, malformations and abnormalities, other than those of diagnostic criteria of VATER association, have been considered significant for clarifying the nature of VATER association and for establishing guidelines for the treatment of infants with VATER association because they are supposed to be determinants of prognosis. Malformations associated with the eye have, however, scarcely been highlighted in VATER association, although several occurrences have been reported. The authors describe the first case of congenital blepharoptosis co-occurring in a patient with VATER association. The co-occurrence of several malformations in the ipsilateral face and hand of the patient were indicative of their arising from the congeneric pathogenesis. Surgical repair of the blepharoptosis was carried out by eyebrow suspension with fascia lata when the patient was 5 years old; a favorable outcome was achieved in both function and aesthetics.

摘要

VATER 协会是指 5 种特定异常(椎体和血管异常[V]、肛门闭锁[A]、食管闭锁和/或气管食管瘘[TE]、桡骨和肾脏异常[R])在一个个体中同时发生的倾向。最近,除了 VATER 协会的诊断标准之外,其他畸形和异常也被认为对阐明 VATER 协会的性质和制定 VATER 协会婴儿治疗指南很重要,因为它们被认为是预后的决定因素。然而,眼部畸形在 VATER 协会中很少被强调,尽管已经有报道了一些病例。作者描述了首例先天性上睑下垂伴 VATER 协会的病例。患者同侧面部和手部的多种畸形并存,提示其具有同源性发病机制。当患者 5 岁时,通过用阔筋膜进行眉悬吊术对其进行了上睑下垂的手术修复;在功能和美学方面均取得了良好的效果。

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