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1型Stickler综合征同卵双胞胎中的视网膜脱离

Retinal detachment in identical twins with Stickler syndrome type 1.

作者信息

Watanabe Y, Ueda M, Adachi-Usami E

机构信息

Department of Ophthalmology, Chiba University School of Medicine, Japan.

出版信息

Br J Ophthalmol. 1996 Nov;80(11):976-81. doi: 10.1136/bjo.80.11.976.

DOI:10.1136/bjo.80.11.976
PMID:8976725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC505675/
Abstract

BACKGROUND

The high incidence of retinal detachment and its poor surgical prognosis in patients with Stickler syndrome are well known. However, the vitreoretinal relation to retinal detachment in this syndrome is uncertain.

METHODS

Vitreoretinal examination with a binocular indirect ophthalmoscope and a Goldmann three mirror contact lens was performed on identical twin boys with Stickler syndrome. Each had retinal detachment in the left eye, and many aspects of their fundus findings were similar. The vitreous showed distinct abnormalities consistent with congenital vitreous anomaly of type 1 Stickler syndrome. The twins were followed up for 4 years after undergoing a successful operation to reattach their left retinas.

RESULTS

Rhegmatogenous detachment with multiple tears occurred in the right eye of only one twin during the follow up period, despite the similar condition of their fundi. Although vitreous body was not present in most parts, slightly opaque vitreous cortex was attached to the retina near the ora serrata, and neither twin had posterior vitreous detachment during the follow up period.

CONCLUSION

Multiple retinal tears appeared simultaneously in the right eye of one twin, indicating some tractional force had acted on the retina. It is believed that this force was caused by very thin vestigial vitreous cortex attached to the retina. Although these observations have been limited, vitreoretinal findings of the twins and their father were consistent and suggested presence of thin vitreous cortex attached to the retina without posterior vitreous detachment.

摘要

背景

史迪综合征患者视网膜脱离的高发病率及其较差的手术预后是众所周知的。然而,该综合征中玻璃体视网膜与视网膜脱离的关系尚不确定。

方法

对患有史迪综合征的同卵双胞胎男孩进行双目间接检眼镜和戈德曼三面镜接触镜的玻璃体视网膜检查。两人左眼均有视网膜脱离,且眼底检查的许多方面相似。玻璃体显示出与1型史迪综合征先天性玻璃体异常一致的明显异常。这对双胞胎在成功进行左眼视网膜复位手术后随访了4年。

结果

在随访期间,仅其中一名双胞胎的右眼发生了伴有多个裂孔的孔源性视网膜脱离,尽管他们的眼底情况相似。尽管大部分区域玻璃体已不存在,但在锯齿缘附近仍有轻度混浊的玻璃体皮质附着于视网膜,且在随访期间两人均未发生玻璃体后脱离。

结论

一名双胞胎的右眼同时出现多个视网膜裂孔,表明有某种牵拉力作用于视网膜。据信这种力是由附着于视网膜的非常薄的残留玻璃体皮质引起的。尽管这些观察结果有限,但这对双胞胎及其父亲的玻璃体视网膜表现是一致的,提示存在附着于视网膜且无玻璃体后脱离的薄玻璃体皮质。

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引用本文的文献

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Stickler Syndrome (SS): Laser Prophylaxis for Retinal Detachment (Modified Ora Secunda Cerclage, OSC/SS).斯迪克勒综合征(SS):视网膜脱离的激光预防(改良的锯齿缘环扎术,OSC/SS)
Clin Ophthalmol. 2021 Jan 6;15:19-29. doi: 10.2147/OPTH.S284441. eCollection 2021.
2
Targeted next‑generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment.靶向下一代测序鉴定出伴双侧视网膜脱离的斯蒂克勒综合征中 COL2A1 基因的两个新突变。
Int J Mol Med. 2018 Oct;42(4):1819-1826. doi: 10.3892/ijmm.2018.3752. Epub 2018 Jul 4.

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