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努南综合征中的自发性角膜破裂。病例报告。

Spontaneous corneal rupture in Noonan syndrome. A case report.

作者信息

Au Y K, Collins W P, Patel J S, Asamoah A

机构信息

Department of Ophthalmology, Louisiana State University Medical School- Shreveport 71130-3932, USA.

出版信息

Ophthalmic Genet. 1997 Mar;18(1):39-41. doi: 10.3109/13816819709057882.

DOI:10.3109/13816819709057882
PMID:9134549
Abstract

PURPOSE/METHODS: A variety of ocular and periocular manifestations have been described in Noonan syndrome. Collagen abnormalities have been described; however, to our knowledge spontaneous corneal rupture has not been reported. A forty-three-year-old female who presented with spontaneous corneal rupture was later diagnosed as having Noonan syndrome.

RESULTS/CONCLUSIONS: Collagen abnormalities have been described with Noonan syndrome and this is likely the cause of corneal rupture in this patient.

摘要

目的/方法:努南综合征有多种眼部及眼周表现。已有胶原异常的相关描述;然而,据我们所知,自发性角膜破裂尚未见报道。一名43岁女性因自发性角膜破裂就诊,后来被诊断为努南综合征。

结果/结论:努南综合征存在胶原异常,这可能是该患者角膜破裂的原因。

相似文献

1
Spontaneous corneal rupture in Noonan syndrome. A case report.努南综合征中的自发性角膜破裂。病例报告。
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引用本文的文献

1
Ocular manifestations of Noonan syndrome in twin siblings: a case report of keratoconus with acute corneal hydrops.双胞胎姐弟努南综合征的眼部表现:圆锥角膜伴急性角膜水肿病例报告
Indian J Ophthalmol. 2014 Dec;62(12):1171-3. doi: 10.4103/0301-4738.126992.
2
Aneurysmal sub-arachnoid haemorrhage in patients with Noonan syndrome: a report of two cases and review of neurovascular presentations in this syndrome.努南综合征患者的动脉瘤性蛛网膜下腔出血:两例报告及该综合征神经血管表现的综述
Neuroradiology. 2004 Apr;46(4):301-5. doi: 10.1007/s00234-004-1185-3. Epub 2004 Mar 18.