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无可见眼底异常的遗传性黄斑营养不良

Hereditary macular dystrophy without visible fundus abnormality.

作者信息

Miyake Y, Ichikawa K, Shiose Y, Kawase Y

机构信息

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

出版信息

Am J Ophthalmol. 1989 Sep 15;108(3):292-9. doi: 10.1016/0002-9394(89)90120-7.

Abstract

We found an unusual form of macular dystrophy in three patients from two generations of the same family. The fundi of these patients appeared normal by ophthalmoscopy and fluorescein angiography, even in an older patient and in patients with poor visual acuity. Results of full-field electroretinograms were also normal in both cone and rod components. Focal macular electroretinograms were severely affected, however, indicating retinal impairment in the macular region. Results of Tübingen perimetry were consistent with electroretinographic findings. Since the condition was progressive, this disease is thought to be a hereditary macular dystrophy without visible fundus abnormality.

摘要

我们在来自同一家族两代人的三名患者中发现了一种不寻常形式的黄斑营养不良。通过检眼镜检查和荧光素血管造影,这些患者的眼底看起来正常,即使是老年患者和视力较差的患者也是如此。全视野视网膜电图的结果在视锥和视杆成分中也均正常。然而,局部黄斑视网膜电图受到严重影响,表明黄斑区域存在视网膜损伤。图宾根视野检查的结果与视网膜电图检查结果一致。由于病情呈进行性发展,这种疾病被认为是一种无可见眼底异常的遗传性黄斑营养不良。

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