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基因和病理确诊的脑腱黄瘤病一例 被引量:6

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摘要 脑腱黄瘤病(cerebrotendinousxanthomatosis,CTX)是由CYP27A1基因突变引起的罕见的常染色体隐性遗传病.CTX发病率低,临床表现多样,易被误诊、漏诊.自1937年VonBogaert等报道首例CTX以来,全球报道的CTX仅数百例,国内报道仅14例[1].现将我们收治的1例经基因和病理确诊的CTX患者报道如下.
出处 《中华神经科杂志》 CAS CSCD 北大核心 2017年第5期372-374,共3页 Chinese Journal of Neurology
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  • 1袁云,王朝霞,张巍,冯立群.脑腱黄瘤病的周围神经改变一家系分析[J].中华神经科杂志,2005,38(3):195-197. 被引量:13
  • 2Chang WN, Kuriyama M, Lui CC, et al. Cerebrotendinous xanthomatosis in three siblings from a Taiwan Residents family.J Formos Med Assoc, 1992, 91: 1190-1194.
  • 3Moghadasian MH, Salen G, Frohlich JJ, et al. Cerebrotendinous xanthomatosis: a rare disease with diverse manifestations. Arch Neurol, 2002, 59: 527-529.
  • 4Lee Y, Lin PY, Chiu NM, et al. Cerebrotendinous xanthomatosis with psychiatric disorders: report of three siblings and literature review. Chang Gung Med J, 2002, 25: 334-340.
  • 5Dotti MT, Rufa A, Federico A. Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings. J Inherit Metab Dis, 2001, 24: 696-706.
  • 6Kuritzky A, Berginer VM, Korczyn AD. Peripheral neuropathy in cerebrotendinous xanthomatosis. Neurology, 1979, 29: 880-881.
  • 7Ohnishi A, Yamashita I, Goto Y, et al. De- and remyelination and oninon bulb in cerebrotendinous xanthomatosis. Acta Neuropathol (berl), 1979, 45: 43-45.
  • 8Berginer VM, Salen G, Shefer S. Long-term treatment of cerebrotendinous xanthomatosis with chenodeoxycholic acid. N Engl J Med, 1984, 311: 1649-1652.
  • 9Tokimura Y, Kuriyama M, Arimura K, et al. Electrophysiological studies in cerebrotendinous xanthomatosis. J Neurol Neurosurg Psychiatry, 1992, 55: 52-55.
  • 10Verrips A, van Engelen BG, ter Laak H, et al. Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients. Neuromuscul Disord, 2000, 10: 407-414.

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