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J-GLOBAL ID:201702237925700016   Reference number:17A0111389

ミトコンドリア病と鑑別を要する臨床表現型を呈しCYP27A1遺伝子エクソン1に新規フレームシフト変異(c. 43_44delGG)を認めた脳腱黄色腫症の1例

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Material:
Volume: 56  Issue: 10  Page: 667-671(J-STAGE)  Publication year: 2016 
JST Material Number: U0602A  ISSN: 1882-0654  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Diagnostics of metabolic diseases,nutritional diseases.  ,  Neurologic diagnosis  ,  Genetic variation 
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Reference (16):
  • 1) Gallus GN, Dotti MT, Federico A, et al. Clinical and molecular diagnosis of cerebrotendinous xanthomatosis with a review of the mutation in the CYP27A1 gene. Neurol Sci 2006;27:143-149.
  • 2) 野末 剛.脳腱黄色腫症の遺伝子解析とケノデオキシコール酸による治療効果に関する研究.金沢大十全医会誌 2002;111:20-34.
  • 3) Menkes JH, Schimschock JR, Swanson PD. Cerebrotendinous xanthomatosis: the storage of cholestanol within the nervous system. Arch Neurol 1968;19:47-53.
  • 4) Oftebro H, Björkhem I, Skrede S, et al. Cerebrotendinous xanthomatosis; a defect in mitochondrial 26-hydroxylation required for normal biosynthesis of cholic acid. J Clin Invest 1980;65:1418-1430.
  • 5) de la Fuente BP, Sobrido MJ, Girós M, et al. Usefulness of cholestanol levels in the diagnosis and follow-up of patients with cerebrotendinous xanthomatosis. Neurologia 2011;26:397-404.
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