显性青少年型视神经萎缩
Dominant juvenile optic atrophy.
作者信息
Neetens A, Rubbens M C
出版信息
Ophthalmic Paediatr Genet. 1985 Feb;5(1-2):79-83. doi: 10.3109/13816818509007859.
PMID:4058875
Abstract
Optic atrophy beginning in early childhood and accompanied by tritan-type dyschromatopsia, but normal ERG and abnormal VCEP, is described in a family. Differential diagnosis of hereditary optic atrophy is discussed.
摘要
一个家族中描述了始于儿童早期并伴有蓝色盲型色觉异常，但视网膜电图正常而视觉诱发电位异常的视神经萎缩情况。文中讨论了遗传性视神经萎缩的鉴别诊断。
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