Focal parafoveal retinal telangiectasis.
Focal parafoveal retinal telangiectasis.
复制标题
局灶性中心凹旁视网膜毛细血管扩张。
DOI：
--
复制
发表时间：
1978
期刊：
影响因子：
--
通讯作者：
A. Vaiser
中科院分区：
文献类型：
--
作者：
W. L. Hutton;W. Snyder;D. Fuller;A. Vaiser
我们描述了四名患者，其中两人是姐妹，他们患有一种不寻常的视网膜毛细血管扩张。血管异常局限于颞叶中央凹旁视网膜，每个患者的外观几乎相同。其他特征包括：男性和女性都受累，双眼通常受到影响，症状在中年出现。激光光凝术成功地提高了治疗眼的视力。这些病例的外观和位置的一致性以及家族性倾向表明这些病例可能形成视网膜毛细血管扩张症的一个亚群。
We describe four patients, two of whom are sisters, with an unusual form of retinal telangiectasis. The vascular abnormality is localized to the temporal parafoveal retina and is virtually identical in appearance in every patient. Other characteristics include: both men and women are involved, both eyes are generally affected, and symptoms develop in middle life. Laser photocoagulation succeeds in improving the visual acuity in the treated eyes. The consistency of the appearance and location, and the familial tendency indicates these cases probably form a subgroup of retinal telangiectasis.