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甲亢性周期性麻痹的遗传易感基因研究进展 被引量:2

The Research Progress of Heredity Predisposing Genes of Thyrotoxic Periodic Paralysis
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摘要 甲亢性周期性麻痹(TPP)是甲亢的一种合并症,其发生存在着明显的性别和种族差异,由于遗传因素与环境因素相互作用而发病。本文简单介绍了TPP的临床特征和流行病学,报告了与其可能相关的易感基因。 Thyrotoxic periodic paralysis (TPP) is a complication of hyperthyroidism. The development of TPP has evident discrepancy of sex and race of people, its onset is due to the interaction of genetic factor and environmental factor. Our article simply introduces the clinical feature and epidemiology of TPP, and reports the possible correlative predisposing genes of TPP.
出处 《医学综述》 2006年第5期266-267,共2页 Medical Recapitulate
关键词 甲状腺功能亢进症 周期性麻痹 基因 Hyperthyroidism Periodic paralysis Gene
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参考文献16

  • 1Liu YC ,Tsai WS, Chau T, et al. Acute hypercapnic respiratory failure due to thyrotoxic periodic paralysis[ J ]. Am J Med Sci, 2004,327 (5) :264-267.
  • 2Tassone H, Moulin A, Henderson SO. The pitfalls of potassium replacement in thyrotoxic periodic paralysis : a case report and review of the literature[J] .J Emerg Med,2004,26(2) :157-161.
  • 3Chatot-Henry C, Smadia D, Longhi R, et al. Thymtoxic periodic paralrsis : two new cases in blacks [ J ]. Rev Med Interne, 2000,21 (7) : 632-634.
  • 4江蓓,张宝珠.甲亢肌病的表现及其处理[J].中国实用内科杂志,1997,17(12):713-714. 被引量:159
  • 5Dixon AN, Jones R. Thyrotoxic periodic paralysis in a white woman[ J ].Postgrad Med J,2002,78(925) :687-688.
  • 6Nellen H, Mercado M, Mendoza V, et al. Thyrotoxic periodic paralysis in Mexican mestizo patients: a clinical, biochemical and HLA-semlogical study [J]. Arch Med Res, 1999,30( 1 ) : 74-76.
  • 7李进,张秀清,田苇.甲亢合并周期性麻痹53例分析[J].现代中西医结合杂志,2002,11(14):1342-1343. 被引量:3
  • 8Chen L, Lang D, Ran XW, et al. Clinical and molecular analysis of chinese patients with thyrotoxic periodic paralysis[ J]. Eur Neurol, 2003,49(4) : 227-230.
  • 9Ng WY,Lui KF,Thai AC, et al, Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis[J].Thyroid, 2004,14(3) : 187-190.
  • 10Lin SH, Hsu YD, Cheng NL, et al. Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis[ J]. Am J Mod Sci, 2005,329(2) :66-70.

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