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下颌面骨发育不全中的泪道异常

Lacrimal drainage anomalies in mandibulofacial dysostosis.

作者信息

Bartley G B

机构信息

Department of Ophthalmology, Mayo Clinic, Rochester, MN 55905.

出版信息

Am J Ophthalmol. 1990 May 15;109(5):571-4. doi: 10.1016/s0002-9394(14)70688-9.

DOI:10.1016/s0002-9394(14)70688-9
PMID:2333920
Abstract

Seven patients who had the complete form of mandibulofacial dysostosis were examined to determine the prevalence of nasolacrimal abnormalities. Bilateral inferior punctal atresia (and, by implication, accompanying inferior canalicular atresia) was identified in all seven patients; a 95% confidence interval for the true underlying rate of this finding in mandibulofacial dysostosis is 59% to 100%. Lacrimal surgery was required in only one patient who had coexistent bilateral nasolacrimal duct obstruction and chronic dacryocystitis and who responded well to bilateral dacryocystorhinostomy.

摘要

对7例患有完全型下颌面骨发育不全的患者进行了检查,以确定鼻泪异常的患病率。在所有7例患者中均发现双侧下泪点闭锁(并由此推断伴有下泪小管闭锁);在患有下颌面骨发育不全的患者中,这一发现的真实潜在发生率的95%置信区间为59%至100%。仅1例同时患有双侧鼻泪管阻塞和慢性泪囊炎且对双侧泪囊鼻腔吻合术反应良好的患者需要进行泪道手术。

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引用本文的文献

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Treacher Collins syndrome: A case report and review of ophthalmic features.特雷彻·柯林斯综合征:一例病例报告及眼科特征综述。
Taiwan J Ophthalmol. 2016 Oct-Dec;6(4):206-209. doi: 10.1016/j.tjo.2016.07.002. Epub 2016 Aug 12.
2
Ophthalmic features and visual prognosis in the Treacher-Collins syndrome.特雷彻-柯林斯综合征的眼部特征及视觉预后
Br J Ophthalmol. 1993 Oct;77(10):642-5. doi: 10.1136/bjo.77.10.642.