Hutton W L, Snyder W B, Fuller D, Vaiser A
Arch Ophthalmol. 1978 Aug;96(8):1362-7. doi: 10.1001/archopht.1978.03910060116003.
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.
我们描述了四名患有一种不寻常形式视网膜毛细血管扩张症的患者，其中两名是姐妹。血管异常局限于颞侧黄斑旁视网膜，且在每位患者中的外观几乎相同。其他特征包括：男女均受累，双眼通常均受影响，症状在中年时出现。激光光凝术成功提高了治疗眼的视力。外观和位置的一致性以及家族倾向表明，这些病例可能构成视网膜毛细血管扩张症的一个亚组。
