复视
脊髓小脑共济失调
会聚(光学)
马查多-约瑟夫病
眼球运动
医学
眼科
听力学
共济失调
心理学
光学
物理
精神科
作者
Yasumasa Ohyagi,Takeshi Yamada,Akira Okayama,Nobutaka Sakae,Takao Yamasaki,T. Ohshima,Taiji Sakamoto,Naoki Fujii,Jun‐ichi Kira
标识
DOI:10.1016/s0022-510x(99)00309-3
摘要
Diplopia, a common symptom in spinocerebellar ataxia 3/Machado–Joseph disease (SCA3/MJD) cases, is not always due to asymmetric ophthalmoplegia. We found a Japanese SCA3/MJD family, in which three patients clearly had an impairment of divergence eye movement. We thus quantitatively examined the vergence ranges in eight Japanese SCA3/MJD cases using the synoptophore test. An impairment of the vergence eye movements was found in all patients, and the vergence impairment pattern, but not the ophthalmoplegia pattern, was found to be compatible with the diplopia pattern. The diplopia in SCA3/MJD cases is, therefore, attributed, at least in part, to the impairment of the vergence eye movements.
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