Savell J, Cook J R
Arch Ophthalmol. 1976 Mar;94(3):395-400. doi: 10.1001/archopht.1976.03910030183002.
Fifteen members of a family had congenital colobomas of the optic nerves, all of which were bilateral. The bolobomas appeared as enlargement of the physiologic cup with severely affected eyes having huge cavities in the site of the disc. A variable amount of glial tissue was present within the colobomas. Either macular or extramacular serous detachment or sequelae were present in 21 of the 30 affected eyes, and often led to total blindness. Radioisotope cisternography in one patient failed to implicate cerebrospinal fluid as the source of the subretinal fluid. The disorder is apparently inherited as an autosomal dominant.
一个家族中的15名成员患有先天性视神经缺损,均为双侧性。缺损表现为生理杯扩大,病情严重的眼睛视盘部位有巨大空洞。缺损内有数量不等的胶质组织。30只患眼中有21只出现黄斑或黄斑外浆液性脱离或后遗症,常导致完全失明。一名患者的放射性核素脑池造影未显示脑脊液是视网膜下液的来源。该疾病显然以常染色体显性方式遗传。