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作为一种掩蔽疗法,在家族性自主神经异常患者中使用美容性双色隐形眼镜。

Piggyback cosmetic contact lens as an occlusion therapy in a patient with familial dysautonomia.

机构信息

É cole d'optométrie- Univeristé de Montré al (L.M.), Montréal,Québec, Canada.

出版信息

Eye Contact Lens. 2010 Nov;36(6):367-70. doi: 10.1097/ICL.0b013e3181f57aed.

DOI:10.1097/ICL.0b013e3181f57aed
PMID:20935568
Abstract

PURPOSE

The purpose of this case report is to explore the treatment of ocular and visual complications secondary to familial dysautonomia (Riley–Day syndrome) on an 8 month-old baby. Treatments for corneal scarring,ocular protection, and amblyopia were achieved by fitting a scleral lens with a unique piggyback combination involving a cosmetic soft contact lens.

METHOD

The patient was seen in February 2008, on referral from a corneal specialist, for a scleral lens fitting. This case was comanaged from Université de Montréal with the help of the Boston Foundation for Sight.Examination revealed a right cornea with opacities. We planned to use scleral lenses to treat this eye and to protect the other one. Although the patient's ocular condition did improve, some concerns arose about potential impact on her visual development. Our treatment for amblyopia involved the use of atropine in both eyes and penalization of the good eye with a cosmetic opaque contact lens that we fitted onto a piggyback system over the scleral lens. The rationale behind this approach is explained in this article.

RESULT

After the contact lens was fitted and after penalization and atropinization,the baby's visual condition improved. Time will tell to what degree this treatment is effective.

CONCLUSION

Familial dysautonomia is a challenging condition for the eye because of the presence of alacrymia and lack of corneal sensitivity. Scleral contact lenses and cosmetic contact lenses offer a unique way of addressing many issues, such as corneal healing and amblyopia, raised in this case report. These devices may be considered for any other case that requires corneal tissue healing and visual development.

摘要

目的

本病例报告旨在探讨对家族性自主神经异常(赖利-戴综合征)导致的婴儿 8 月龄眼部和视力并发症的治疗方法。通过使用一种独特的附加组合式巩膜镜来矫正角膜混浊、保护眼部和治疗弱视,从而实现对角膜混浊的治疗。

方法

该患者于 2008 年 2 月因角膜混浊就诊于角膜专家转诊,进行巩膜镜适配。该病例在蒙特利尔大学与波士顿视力基金会的协助下共同管理。检查发现右眼角膜混浊。我们计划使用巩膜镜来治疗该眼,并保护另一只眼。尽管患者的眼部状况有所改善,但对其视觉发育可能产生的影响仍存在一些担忧。我们使用阿托品治疗弱视,并用美容性不透明隐形眼镜遮盖健眼,该隐形眼镜置于巩膜镜的附加系统上。本文对这种治疗方法的原理进行了阐述。

结果

在佩戴隐形眼镜并进行遮盖和散瞳后,婴儿的视力状况得到改善。这种治疗方法的效果程度还有待时间的检验。

结论

家族性自主神经异常对视功能具有挑战性,因为存在无泪症和角膜感觉缺失。巩膜接触镜和美容性接触镜为解决本病例报告中提出的许多问题提供了独特的方法,例如角膜愈合和弱视。对于任何需要角膜组织愈合和视觉发育的病例,都可以考虑使用这些设备。

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Current treatments in familial dysautonomia.
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