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瞳孔缺损性畸形的眼底镜检查演变

Ophthalmoscopic evolution of papillary colobomatous malformations.

作者信息

Villalonga Gornés P A, Galan Terraza A, Gil-Gibernau J J

机构信息

Pediatric Ophthalmologic Unit, Hospital Materno-Infantil, Ciudad Sanitaria Vall D'Hebron, Univ Autonoma of Barcelona, Spain.

出版信息

J Pediatr Ophthalmol Strabismus. 1995 Jan-Feb;32(1):20-5. doi: 10.3928/0191-3913-19950101-06.

Abstract

We describe congenital colobomatous malformations of the optic nerve and the clinical variations and complications that may appear eventually in them. We also present two clinical cases of patients with papillary colobomatous defects where spontaneous variations have been observed throughout their evolution and where the current ophthalmoscopic aspect is completely different from the initial one. Finally, bearing in mind the embryologic origin and histologic structure of these anomalies, we develop a hypothesis that explains the physiopathologic mechanism that causes the clinical changes described in each case.

摘要

我们描述了先天性视神经缺损畸形以及最终可能出现的临床变异和并发症。我们还展示了两例患有乳头缺损的患者的临床病例,在其整个病程中观察到了自发变异,且当前的检眼镜检查结果与最初完全不同。最后,考虑到这些异常的胚胎学起源和组织结构,我们提出了一个假说,解释了导致每个病例中所描述临床变化的病理生理机制。

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