期刊文献+

HNRNPU基因杂合突变致神经发育综合征一例并文献复习 被引量:1

下载PDF
导出
摘要 异质核糖核蛋白U(heterogeneousnuclearribonucle oprotein U,hnRNP U)又被称为支架附着因子A(scaffold attachment factor A,SAF-A),属于异质核糖核蛋白亚家族,在胎儿大脑、成人心脏、肾脏、肝脏、大脑和小脑中表达,在哺乳动物的发育中起着至关重要的作用。HNRNPU基因编码异质核蛋白U,该基因定位于染色体1q44区域内,该区域的DNA改变可引起常染色体1q43-q44缺失综合征,出现发育迟缓、智力障碍、小头畸形、癫痫发作、畸形面部特征、胼胝体发育不良、以及心脏、肾脏发育畸形等临床表现。
出处 《海南医学》 CAS 2021年第17期2298-2300,共3页 Hainan Medical Journal
  • 相关文献

参考文献2

二级参考文献54

  • 1Thomas RH, Berkovic SF. The hidden genetics of epilepsy-a clinically important new paradigm [ J]. Nat Rev Neurol, 2014, 10 (5) :283-292.
  • 2Martin HC, Kim GE, Pagnamenta AT, et al. Clinical whole-ge- nome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis [J]. Hum Mol Genet, 2014,23 (12) : 3200-3211.
  • 3Rossi S, Daniele I, Bastrenta P, et al. Early myoclonic enceph- alopathy and nonketotic hyperglycinemia [J]. Pediatr Neurol, 2009,41 (5) : 371-374.
  • 4Azize NA, Ngah WZ, Othman Z, et al. Mutation ana!ysis of gly- cine decarboxylase, aminomethyhransferase and glycine cleav- age system protein-H genes in 13 unrelated families with gly- cine encephalopathy[J]. J Hum Genet, 2014,59( 11 ) : 593-597.
  • 5Kim JH, Lee BH, Kim YM, et al. Novel mutations and clinical outcomes of copper- histidiue therapy in Menkes disease pa- tients [ J ]. Metab Brain Dis, 2015,30 ( 1 ) : 75-81.
  • 6Rosewich H, Waterham H, Poll-The BT, et al. Clinical utility gene card for Zellweger syndrome spectrum[J]. Eur J Hum Gen- et,2014,11 (19) : el-e4.
  • 7Cohen R, Basel-Vanagaite L, Goldberg-Stern H, et al. Two sib- lings with early infantile myoclonic encephalopathy due to muta- tion in the gene encoding mitochondrial glutamate/H+symporter SLC25A22 [ J ]. Eur J Paediatr Neurol, 2014,18 (6) : 801-805.
  • 8Backx L, Ceulemans B, Vermeesch JR, et al. Early myoclonic encephalopathy caused by a disruption of the neuregulin- 1 re-ceptor ErbB4 [J ]. Eur J Hum Genet, 2009,17 (3) : 378-382.
  • 9Kato M, Saitsu H, Murakami Y, et al. PIGA mutations cause ear- ly-onset epileptic encephalopathies and distinctive features [J]. Neurology, 2014,82 (18) : 1587-1596.
  • 10Pavone P, Spalice A, Polizzi A, et al. Ohtahara syndrome with emphasis on recent genetic discovery [J ]. Brain Dev, 2012,34 (6) : 459-468.

共引文献14

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