Yamashita T, Kawano K, Ohba N
Department of Ophthalmology, Kagoshima University, Faculty of Medicine, Japan.
Ophthalmic Paediatr Genet. 1988 Mar;9(1):17-24. doi: 10.3109/13816818809031476.
Four members of three consecutive generations of a family had congenital anomalies of the optic disk: deep excavation of the optic disk containing a mass of white glial tissue at its center, anomalous retinal vessels emerging from the peripheral aspect of the disk, and elevated annulus of peripapillary pigmentary disturbance. These optic disk anomalies occurred bilaterally with some inter- and intra-individual variable expressivity. Five of the eight affected eyes had profound visual loss, but three eyes showed normal vision. Two cases developed unilateral nonrhegmatogenous retinal detachment. There were no other ocular or systemic malformations. This family illustrates an instance of autosomal dominantly inherited optic nerve coloboma.
视盘深度凹陷,中央有一团白色神经胶质组织,异常视网膜血管从视盘周边发出,视盘周围色素紊乱的环形区域隆起。这些视盘异常双侧发生,个体间和个体内有一定的可变表达。8只患眼中有5只视力严重丧失,但3只眼视力正常。2例发生单侧非孔源性视网膜脱离。没有其他眼部或全身畸形。这个家族说明了常染色体显性遗传视神经缺损的一个实例。