Hagemoser K, Weinstein J, Bresnick G, Nellis R, Kirkpatrick S, Pauli R M
Department of Medical Genetics, University of Wisconsin-Madison.
Am J Med Genet. 1989 May;33(1):61-5. doi: 10.1002/ajmg.1320330108.
Here we report on two families with a previously apparently undescribed, autosomal dominant disorder resulting in optic atrophy and subsequent development of hearing loss and peripheral neuropathy. This disorder differs from previous syndromes resulting in this triad of effects both in the severity and early onset of the optic atrophy and in its mode of transmission. Review of published cases of optic atrophy + hearing loss + peripheral neuropathy suggests that there are at least three such specific disorders; classification of these published cases by first-appearing symptom also results in a clean division by most-likely inheritance.
在此,我们报告了两个家族,其患有一种先前显然未被描述的常染色体显性疾病,该疾病会导致视神经萎缩,随后出现听力丧失和周围神经病变。这种疾病与先前导致这三种症状的综合征不同,无论是在视神经萎缩的严重程度和早期发作方面,还是在其遗传模式上。对已发表的视神经萎缩 + 听力丧失 + 周围神经病变病例的回顾表明,至少存在三种这样的特定疾病;根据首发症状对这些已发表病例进行分类,也会依据最可能的遗传方式进行清晰划分。