Odland M
Acta Ophthalmol (Copenh). 1981 Oct;59(5):649-58. doi: 10.1111/j.1755-3768.1981.tb08730.x.
Four generations of a family with congenital retinoschisis are described. Six male members in the second generation suffer from this disease. The fundus changes in these patients were advanced with marked chorioretinal atrophy. Schisis of the retina was only seen in one of them. Three boys in the fourth generation exhibited retinoschisis with typical macula changes. One had detachment in one eye. ERG was in most cases subnormal or extinguished. Fluorescein angiography showed leakage of dye in 2 patients and one of these had vessel malformation.
本文描述了一个患有先天性视网膜劈裂症的四代家族。第二代中有六名男性成员患有此病。这些患者的眼底病变进展明显，伴有显著的脉络膜视网膜萎缩。仅在其中一名患者中观察到视网膜劈裂。第四代中有三名男孩表现出视网膜劈裂，并伴有典型的黄斑改变。其中一人一只眼睛发生了视网膜脱离。大多数情况下，视网膜电图异常或消失。荧光素血管造影显示2例患者有染料渗漏，其中1例伴有血管畸形。
