Mets M B, Mhoon E
Ophthalmic Paediatr Genet. 1985 Feb;5(1-2):85-9. doi: 10.3109/13816818509007860.
The seventh family manifesting an entity described as automosal dominant optic atrophy with hearing loss is reported here. This disorder shows great inter- and intrafamilial variation in the onset time and the degree of loss of both vision and hearing. Unlike autosomal dominant optic atrophy without hearing loss, it appears to be associated with a red-green (deutan) defect in color vision.
本文报告了第七个表现为一种被描述为伴有听力丧失的常染色体显性遗传性视神经萎缩的家系。这种疾病在发病时间以及视力和听力丧失程度方面,在家族间和家族内均表现出很大差异。与不伴有听力丧失的常染色体显性遗传性视神经萎缩不同,它似乎与红绿色(绿色盲)色觉缺陷有关。