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1型神经纤维瘤病患者的超常眼电图

Supernormal electro-oculograms in patients with neurofibromatosis type 1.

作者信息

Lubiński Wojciech, Zajaczek Stanisław, Sych Zbigniew, Penkala Krzysztof, Palacz Olgierd, Lubiński Jan

机构信息

Clinic of Ophthalmology, Pomeranian Medical University, Szczecin, Poland.

出版信息

Hered Cancer Clin Pract. 2004 Sep 15;2(4):193-6. doi: 10.1186/1897-4287-2-4-193.

Abstract

PURPOSE

To asses the retinal pigment epithelium (RPE) function measured by EOG testing in patients with neurofibromatosis type 1 (NF-1). Our preliminary EOG results suggested dysfunction of the RPE in individuals with NF-1. In order to confirm our initial results we performed EOG examination on a larger group of NF-1 patients.

PATIENTS

Studies were performed on 36 patients with clinically diagnosed NF-1 and compared to normal healthy controls.

METHODS

Standard EOG recordings were performed in accordance with the International Society for Clinical Electrophysiology of Vision (ISCEV) standards.

RESULTS

In NF-1 patients the Arden indexes of the EOG test were significantly higher primarily due to the lower values of dark troughs. Supernormal EOGs (exceeding the value of the mean + 2 SD from the control group) were present in 58% of NF-1 patients.

CONCLUSIONS

Dysfunction of the RPE is a characteristic feature of individuals with NF-1.

摘要

目的

通过眼电图(EOG)检测评估1型神经纤维瘤病(NF-1)患者的视网膜色素上皮(RPE)功能。我们初步的EOG结果提示NF-1患者存在RPE功能障碍。为了证实我们的初步结果,我们对更大组的NF-1患者进行了EOG检查。

患者

对36例临床诊断为NF-1的患者进行了研究,并与正常健康对照者进行比较。

方法

按照国际临床视觉电生理学会(ISCEV)标准进行标准EOG记录。

结果

NF-1患者EOG检测的 Arden指数显著更高,主要是由于暗谷值较低。58%的NF-1患者存在超常EOG(超过对照组平均值+2标准差的值)。

结论

RPE功能障碍是NF-1患者的一个特征性表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f01a/2840006/4963a7095216/1897-4287-2-4-193-1.jpg

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