期刊文献+

全身性癫癎伴热性惊厥附加症一个家系23例报告 被引量:1

下载PDF
导出
摘要 目的 探讨全身性癫癎伴热性惊厥附加症(generalized epilepsy with febrile seizures pIus,GEFS)的临床和遗传特点。方法对一个家系23例患者的临床资料进行回顾性分析。结果 男:女为1.56:1,患者起病年龄6个月至2.5岁。1例5岁和1例4岁的男孩现在仍有癫癎发作,有3例患者在20岁以后仍有发作,其余18例在10~12岁以后停止发作。发热时可出现癫癎发作,也有不发热时癫癎发作,发作形式多样,除外2例分别4岁和5岁男孩,其余21例患者不用抗癫癎药物能自行停止发作。家系分析显示本病呈常染色体显性遗传。结论 本组病例均于儿童时起病,病程持续时间长短不一,男性多于女性,遗传方式为常染色体显性遗传,21例患者已经自行停止发作,预后良好。
出处 《中国神经精神疾病杂志》 CAS CSCD 北大核心 2004年第5期375-376,共2页 Chinese Journal of Nervous and Mental Diseases
  • 相关文献

参考文献4

  • 1Scheffer IE, Berkovic SF. Generalized epilepsy with febrile seizures plus:A genetic disorder with heterogeneous clinical phenotypes. Brain, 1997,120(3) :479.
  • 2Sinfh R, Scheffer IE, Crossland K, et al. Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome. Ann Neurol, 1999, 45(1):75.
  • 3Gardiner M, Lehesjoki AE. Genetics of epilepsies. Curr Opin Neurol,2000, 13(2): 157.
  • 4Baulac S, Gourfinkel A, Picard F, et al. Asecond locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q-21-q33. Am J Hum Genet, 1999, 65(6): 1078.

同被引文献14

  • 1王家勤,尹景岗,黄希顺,郭学鹏.全面性癫癎伴热性惊厥附加症一家系随访分析[J].实用儿科临床杂志,2004,19(8):679-681. 被引量:6
  • 2席妹景,黄希顺,魏建科,张子英,郑红,常秀红,高磊,樊玉香,王家勤,郭学鹏,尹景岗.全面性癫伴热性惊厥附加症6家系SCN1B基因突变筛查[J].实用儿科临床杂志,2007,22(10):768-770. 被引量:9
  • 3Scayg A,MacDonald BT,Meisler MH. Mutations of SC.N1 A,encoding a neuronal sodium channel,in two families with GEFS +2[J].Nature Genetics,2000,(04):343-345.doi:10.1038/74159.
  • 4Sugawara T,Tsurubuchi Y,Agarwala KL. A missense mutation of the Na + channel alpha Ⅱ subunit gene Na(v) 1.2 in a patient with febrile and afebrile seizures causes channel dysfunction[J].Proceedings of the National Academy of Sciences(USA),2001,(11):63846389.
  • 5Dibbens LM,Feng H J,Richards M C. GABRD encoding a protein for extra-or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies[J].Human Molecular Genetics,2004,(1 3):1315-1319.
  • 6Baulac S,Huberfeld G,Gourfinkel-An I. First genetic evidence of GABA(A) receptor dysfunction in epilepsy:a mnutation in the gamma2-subunit gene[J].Nature Genetics,2001,(01):46-48.doi:10.1038/88254.
  • 7Engel J. International League Against Epilepsy.A proposed diagnostic scheme for people with epileptic seizures and with epilepsy:report of the ILAE Task Force on Classification and Terminnlogy[J].Epilepsia,2001,(06):796-803.doi:10.1046/j.1528-1157.2001.10401.x.
  • 8Wallace RH,Scheffer IE,Barnett S. Neuronal sodium-channel alphal-subunit mutations in generalized epilepsy with febrile seizures plus[J].American Journal of Human Genetics,2001,(04):859-865.
  • 9Scheffer IE,Harkin LA,Dibbens LM. Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS +)[J].Epilepsia,2005,(Suppl 10):41-47.
  • 10Ito M,Nagafuji H,Okazawa H. Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na +)-channel alpha 1 subunitgene,SCN1 A[J].Epilepsy Research,2002,(1-2):15-23.

引证文献1

二级引证文献1

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