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遗传性压力敏感性周围神经病 被引量:5

Hereditary Neuropathy with Liability to Pressure Palsies
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摘要 遗传性压力敏感性周围神经病(HNPP)是一种常染色体显性遗传的周围神经病。HNPP的分子基础是染色体17p11.2区的一个1.5Mb片段缺失。临床特点为反复发作的在易卡压部位神经受压后,受累神经所支配区域出现运动感觉障碍。本病早期准确诊断后采取预防措施可减少发作。本文就HNPP的病因、临床特点及诊断等作一综述。 Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant peripheral neuropathy. The molecular basis of the disease is a deletion of the 1.5-megabase segment on chromosome 17pl 1.2. It is characterized by recurrent transient nerve palsies that occur at sites subject to compression, an early and accurate diagnosis for HNPP can promote preventive measures to avoid nerve pressure, so that recurrent nerve palsies can be reduced. The causes, clinical features and diagnosis are reviewed here.
作者 刘黔云 王毅
出处 《中国临床神经科学》 2009年第4期431-435,共5页 Chinese Journal of Clinical Neurosciences
关键词 遗传性压力敏感性周围神经病 周围神经病 遗传性疾病 hereditary neuropathy with liability to pressure palsies peripheral neuropathy hereditary neuropathy
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参考文献39

  • 1De Jong JGY.Over families met hereditaire dispositie tot het optreden van neuritiden gecorreleered met migraine[J].Psychiatr Neurol Bu11,1947,50:60-76
  • 2Chance PF,Aiderson MK,Leppig KA,et al.DNA deletion associated with hereditary neuropathy with liability to pressure palsiesJ].Cell,1993,72:143-151
  • 3Nelis E,Van Broeckhoven C,De Jonghe P,et al.Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hererditaty neuropathy with liability to pressure palsies:a European collaborative study[J].Eur J Hum Genet,1996,4:25-33
  • 4Sanahuja J,Franco E,Rojas-Garcia R,et al.Central nervous system involvement in hereditary neuropathy with liability to pressure palsies-description of a large family with this association[J].Arch Neurol,2005,62:1911-1914
  • 5Nicholson GA,Valentijn LJ,Cherryson AK,et al.A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies[J].Nat Genet,1994,6:263-266
  • 6Pareyson D,Taroni F.Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies[J].Curr Opin Neurol,1996,9:348-354
  • 7Bort S,Nelis E,Timmerman V,et al.Mutational analysis of the MPZ,PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies[J].Hum Genet,1997,99:746-754
  • 8Young P,Wiebusch H,Stogbauer F,et al.A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies[J].Neurology,1997,48:450-452
  • 9Sahenk Z,Chen L,Freimer M.A novel PMP22 point mutation causing HNPP phenotype:studies on nerve xenografts[J].Neurology,1998,51:702-707
  • 10Haites NE,Nelis E,Van Broeckhoven C,et al.3rd workshop of the European CMT consortium:54th ENMC international workshop on genotype/phenotype correlations in Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies[J].Neuromuscul Disord,1998,8:591-603

二级参考文献14

  • 1陈琳,郭玉璞.遗传性压迫易感性神经麻痹.见:刘焯霖,梁秀龄,张成,主编.神经遗传病学.第2版.北京:人民卫生出版社,2002.80-84.
  • 2Chance PF, Alderson MK, Leppig KA, et al. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell, 1993, 72:143-151.
  • 3Aarskog NK, Vedeler CA. Real-time quantitative polymerase chain reaction. A new method that detects both the peripheral myelin protein 22 duplication in Charcot-Marie-Tooth type 1A disease and the peripheral myelin protein 22 deletion in hereditary neuropathy with liability to pressure palsies. Hum Genet, 2000, 107:494-498.
  • 4Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCB and the 2^△△Ct method. Methods,2001, 25: 402-408.
  • 5Meretoja P, Silander K, Kalimo H, et al. Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western Finland. Neuromuscul Disord, 1997, 7 : 529-532.
  • 6Simonetti S. Lesion of the anterior branch of axillary nerve in a patient with hereditary neuropathy with liability to pressure palsies.Eur J Neurol, 2000, 7: 577-579.
  • 7Gouider R, LeGuem E, Gugenheim M, et al. Clinical,dectrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11. 2 deletion. Neurology, 1995, 45: 2018-2023.
  • 8Amato AA, Gronseth GS, Callerame KJ, et al. Tomaculous neuropathy: a clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p11.2. Muscle Nerve, 1996, 19 : 16-22.
  • 9Mouton P, Tardieu S, Gouider R, et al. Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion. Neurology, 1999, 52: 1440-1446.
  • 10Madman EC, Gabrcels-Festen AA, van Beersum SE, et al.Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies. Ann Neurol, 1994, 36:650-655.

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