Hoyt C S
Ophthalmology. 1980 Mar;87(3):245-51. doi: 10.1016/s0161-6420(80)35247-0.
Autosomal dominant optic atrophy is an abiotrophy with an insidious onset in the first decade of life. The clinical features of 31 individuals in six pedigrees are detailed in this study. These data suggest that here is considerable intrafamilial and interfamilial expression of dysfunction. Moreover, asymmetry of the visual loss in not unusual. An unexpected result of this study is the previously unreported frequent association of a neural hearing loss with this disorder.
常染色体显性遗传性视神经萎缩是一种在生命的第一个十年隐匿起病的营养障碍性疾病。本研究详细描述了6个家系中31人的临床特征。这些数据表明,功能障碍在家族内和家族间存在相当大的表现差异。此外,视力丧失的不对称并不罕见。这项研究的一个意外结果是,此前未报道过这种疾病常伴有神经性听力损失。