期刊文献+

癫痫的遗传学研究进展 被引量:4

下载PDF
导出
摘要 癫痫是常见脑部疾病之一,可由多种病因引起,具有产生多次发作的持续性倾向,从而导致神经生物、认知、心理及社会等方面的多种后果~[1]。调查显示,我国癫痫患病率为5‰,首次发病年龄以儿童、青少年时期为主~[2]。2010年,国际抗癫痫联盟将癫痫按病因分为遗传性、结构性和代谢性、未知病因3类~[3]。遗传性癫痫是指由已知的或推测的遗传缺陷直接导致的癫痫。大量研究显示,在没有明确的外部获得性因素(如头部创伤,中风,感染等)的癫痫病例中,遗传因素发挥了主要作用~[3]。
出处 《国际检验医学杂志》 CAS 2015年第23期3459-3462,共4页 International Journal of Laboratory Medicine
  • 相关文献

参考文献31

  • 1Eisher RS, Boas WV, Blume W, et al. Epileptic seizures and epi- lepsy: Definitions proposed by the International League against Epilepsy (II.AE) and the International Bureau for Epilepsy (IBE) [J]. Epilepsia,2005,46(4) 1470 472.
  • 2常琳,王小姗.中国癫痫流行病学调查研究进展[J].国际神经病学神经外科学杂志,2012,39(2):161-164. 被引量:200
  • 3Berg AT, Berkovic SF, Brodie M J, et al. Revised terminology and concepts for organization of seizures and epilepsies: report of the II.AE Commission on Classification and Terminology, 2005 2009 [J]. Epilepsia,2010,51(4) :676-685.
  • 4Soldovieri MV, Boutry-Kryza N, Milh M, et al. Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neo- natal epilepsy:first evidence for an altered Channel regulation by syntaxin 1A[J]. Hum Mutat,2014,35(3):356-367.
  • 5Giordano L, Sartori S,Russo S,et al. Familial Ohtahara syndrome due to a novel ARX gene mutation[J]. Am J Med Genet A,2010, 152A(12) :3133 3137.
  • 6Pavone P,Spa[ice A,Potizzi A,et at. Ohtahara syndrome with em phasis on recent genetic discovery[J]. Brain Dev, 2012,34(6): 459 468.
  • 7Ishii A, Shinda M, Okumura A, et al. A recurrent KCNTI muta tion in two sporadic cases with malignant migrating partial sei zures in infancy[J]. Gene,2013,531(2):467-471.
  • 8Carranza Rojo D, Hamiwka L, Mcmahon JM, et al. De novo SCNIA mutations in migrating partia] seizures of infancy[J]. Neurology,201 ], 77(4) :380 383.
  • 9Dhamija R,Wirre]l E,Falcao G,et al. Novel de novo SCN2A mu tation in a child with migrating focal seizures of infancy[J]. Pedi atr Neurol,2013,49(6) :486 488.
  • 10Poduri A,Chopra SS, Neilan EG,et al. Homozygous PLCB1 dele tion associated with malignant migrating partial seizures in infan ey[J]. Epilepsia, 2012,53 (8) : e146-el 50.

二级参考文献52

共引文献209

同被引文献24

  • 1谢华,谢景文,贾正平,王荣,徐娟.抗癫痫药物的合理应用[J].中国药物应用与监测,2007,4(3):61-63. 被引量:6
  • 2Gogou M, Pavlou E, Eboriadou M, et al. Risk factors for obstruc- tive sleep apnea syndrome in genetic epilepsy[ J]. Indian J Pediatr,2016, Jun 27. [ Epub ahead of print]. DOI: 10. 1007/s12098- 016-2183-2.
  • 3Thurman DJ, Beghi E, Begley CE, et al. Standards for epiderrfio- logic studies and surveillance of epilepsy[J]. Epilepsia, 2011, 52 Suppl 7:2-26. DOI:10. llll/j. 1528-1167.2011.03121. x.
  • 4Kim KT, Kim J, Han YJ, et al. Assessment of NMDA receptor genes (GRIN2A, GRIN2B and GRIN2C) as candidate genes in the development of degenerative lumbar scoliosis [ J ]. Exp Ther Med, 2013, 5 (3) :977-981. DOI: 10. 3892/etm. 2013. 910.
  • 5Zhou C, Sun H, Klein PM, et al. Neonatal seizures alter NMDA glutamate receptor GluN2A and 3A subunit expression and function in hippocampal CA1 neurons[J]. Front Cell Neumsci, 2015, 9: 362. DOI : 10. 3389/fncel. 2015. 00362.
  • 6Lozovaya N, Gataullina S, Tsintsadze T, et al. Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model[J]. Nat Commun, 2014, 5:4563. DOI: 10. 1038/ncomms5563.
  • 7彭晓青,欧阳樱君.癫痫患者CYP2C19基因多态性分析[J].中国实用医药,2010,5(5):51-52. 被引量:5
  • 8常琳,王小姗.中国癫痫流行病学调查研究进展[J].国际神经病学神经外科学杂志,2012,39(2):161-164. 被引量:200
  • 9史菁菁,廖清船,于锋.抗癫痫药物的基因组学研究进展[J].中国药房,2013,24(1):89-91. 被引量:7
  • 10姜玉武,谢涵.特发性全面性癫痫的遗传学研究进展[J].北京大学学报(医学版),2013,45(2):186-191. 被引量:21

引证文献4

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部