A hereditary disorder with dementia, spastic dysarthria, vertical eye movement paresis, gait disturbance, splenomegaly, and abnormal copper metabolism.
作者信息
Willvonseder R, Goldstein N P, McCall J T, Yoss R E, Tauxe W N
出版信息
Neurology. 1973 Oct;23(10):1039-49. doi: 10.1212/wnl.23.10.1039.
PMID:4795418
Abstract
摘要
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A hereditary disorder with dementia, spastic dysarthria, vertical eye movement paresis, gait disturbance, splenomegaly, and abnormal copper metabolism.
Neurology. 1973 Oct;23(10):1039-49. doi: 10.1212/wnl.23.10.1039.
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Sibling cases of a degenerative neurological disease associated with hypocupraemia and hypobetalipoproteinaemia.与低铜血症和低β脂蛋白血症相关的退行性神经疾病的同胞病例。
Eur J Pediatr. 1993 Apr;152(4):368-71. doi: 10.1007/BF01956756.
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Movement disorder associated with abnormal copper metabolism and decreased blood antioxidants.与铜代谢异常和血液抗氧化剂减少相关的运动障碍。
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An unusual neurological disorder with abnormal copper metabolism.一种伴有铜代谢异常的罕见神经系统疾病。
J Neurol. 1988 Sep;235(7):397-9. doi: 10.1007/BF00314480.
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[Dermatoglyphics of homo- and heterozygotes for Wilson's disease (hepatolenticular degeneration) (author's transl)].威尔逊氏病（肝豆状核变性）纯合子与杂合子的皮纹学（作者译）
Hum Genet. 1976 Feb 29;31(2):211-8. doi: 10.1007/BF00296148.
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