Murayama K, Adachi-Usami E
Department of Ophthalmology, School of Medicine, Chiba University, Japan.
Doc Ophthalmol. 1989 Jun;72(2):181-8. doi: 10.1007/BF00156708.
Two siblings with Leber's congenital amaurosis had bilateral macular colobomas, nystagmus, extinguished ERGs, and degenerative salt and pepper like changes in the fundus. They had non-recordable or non-meaningful visually evoked cortical potentials in response to both flash and pattern stimuli. The ophthalmic conditions were thought to be inherited as an autosomal recessive trait.
两名患有莱伯先天性黑蒙的兄弟姐妹患有双侧黄斑缺损、眼球震颤、视网膜电图熄灭,以及眼底出现类似椒盐样的退行性改变。他们对闪光和图形刺激均无可记录或无意义的视觉诱发电位。眼科疾病被认为是作为常染色体隐性性状遗传的。