메뉴 건너뛰기




Volumn 128, Issue 13, 2015, Pages 1815-1819

Huntington disease in Asia

Author keywords

China; Genotype; Huntington disease; Phenotype

Indexed keywords

TETRABENAZINE;

EID: 84933556800     PISSN: 03666999     EISSN: None     Source Type: Journal    
DOI: 10.4103/0366-6999.159359     Document Type: Review
Times cited : (27)

References (50)
  • 1
    • 84864749266 scopus 로고    scopus 로고
    • The incidence and prevalence of Huntington’s disease: A systematic review and meta-analysis
    • Pringsheim T, Wiltshire K, Day L, Dykeman J, Steeves T, Jette N. The incidence and prevalence of Huntington’s disease: A systematic review and meta-analysis. Mov Disord 2012;27:1083-91.
    • (2012) Mov Disord , vol.27 , pp. 1083-1091
    • Pringsheim, T.1    Wiltshire, K.2    Day, L.3    Dykeman, J.4    Steeves, T.5    Jette, N.6
  • 2
    • 0028564730 scopus 로고
    • DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence
    • Squitieri F, Andrew SE, Goldberg YP, Kremer B, Spence N, Zeisler J, et al. DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence. Hum Mol Genet 1994;3:2103-14.
    • (1994) Hum Mol Genet , vol.3 , pp. 2103-2114
    • Squitieri, F.1    Andrew, S.E.2    Goldberg, Y.P.3    Kremer, B.4    Spence, N.5    Zeisler, J.6
  • 3
    • 84867484471 scopus 로고    scopus 로고
    • Huntington’s like conditions in China, A review of published Chinese cases
    • Zheng Z, Burgunder JM, Shang H, Guo X. Huntington’s like conditions in China, A review of published Chinese cases. PLoS Curr 2012;4:RRN1302.
    • (2012) PLoS Curr , vol.4
    • Zheng, Z.1    Burgunder, J.M.2    Shang, H.3    Guo, X.4
  • 4
    • 84897918370 scopus 로고    scopus 로고
    • Preliminary analysis of Huntington’s disease in South Korea
    • Shin CW, Choi YJ, Kim M, Jeon BS. Preliminary analysis of Huntington’s disease in South Korea. J Huntingtons Dis 2013;2:83-7.
    • (2013) J Huntingtons Dis , vol.2 , pp. 83-87
    • Shin, C.W.1    Choi, Y.J.2    Kim, M.3    Jeon, B.S.4
  • 5
    • 36549031236 scopus 로고    scopus 로고
    • Analysis of CCG repeats in Huntingtin gene among HD patients and normal populations in Japan
    • Morovvati S, Nakagawa M, Osame M, Karami A. Analysis of CCG repeats in Huntingtin gene among HD patients and normal populations in Japan. Arch Med Res 2008;39:131-3.
    • (2008) Arch Med Res , vol.39 , pp. 131-133
    • Morovvati, S.1    Nakagawa, M.2    Osame, M.3    Karami, A.4
  • 6
    • 34547641372 scopus 로고    scopus 로고
    • Non-choreic movement disorders as initial manifestations of Huntington’s disease
    • Becker N, Munhoz RP, Raskin S, Werneck LC, Teive HA. Non-choreic movement disorders as initial manifestations of Huntington’s disease. Arq Neuropsiquiatr 2007;65:402-5.
    • (2007) Arq Neuropsiquiatr , vol.65 , pp. 402-405
    • Becker, N.1    Munhoz, R.P.2    Raskin, S.3    Werneck, L.C.4    Teive, H.A.5
  • 8
    • 84874959729 scopus 로고    scopus 로고
    • Chinese patients with Huntington’s disease initially presenting with spinocerebellar ataxia
    • Dong Y, Sun YM, Liu ZJ, Ni W, Shi SS, Wu ZY. Chinese patients with Huntington’s disease initially presenting with spinocerebellar ataxia. Clin Genet 2013;83:380-3.
    • (2013) Clin Genet , vol.83 , pp. 380-383
    • Dong, Y.1    Sun, Y.M.2    Liu, Z.J.3    Ni, W.4    Shi, S.S.5    Wu, Z.Y.6
  • 9
    • 0037642346 scopus 로고    scopus 로고
    • A case of adult-onset Huntington disease presenting with spasticity and cerebellar ataxia, mimicking spinocerebellar degeneration
    • Kageyama Y, Yamamoto S, Ueno M, Ichikawa K. A case of adult-onset Huntington disease presenting with spasticity and cerebellar ataxia, mimicking spinocerebellar degeneration. Rinsho Shinkeigaku 2003;43:16-9.
    • (2003) Rinsho Shinkeigaku , vol.43 , pp. 16-19
    • Kageyama, Y.1    Yamamoto, S.2    Ueno, M.3    Ichikawa, K.4
  • 10
    • 84892485010 scopus 로고    scopus 로고
    • Clinical features of Chinese patients with Huntington’s disease carrying CAG repeats beyond 60 within HTT gene
    • Liu ZJ, Sun YM, Ni W, Dong Y, Shi SS, Wu ZY. Clinical features of Chinese patients with Huntington’s disease carrying CAG repeats beyond 60 within HTT gene. Clin Genet 2014;85:189-93.
    • (2014) Clin Genet , vol.85 , pp. 189-193
    • Liu, Z.J.1    Sun, Y.M.2    Ni, W.3    Dong, Y.4    Shi, S.S.5    Wu, Z.Y.6
  • 11
    • 84862768602 scopus 로고    scopus 로고
    • Juvenile Huntington’s disease presenting as difficult-to-treat seizure and the first episode of psychosis
    • Chuo YP, Hou PH, Chan CH, Lin CC, Liao YC. Juvenile Huntington’s disease presenting as difficult-to-treat seizure and the first episode of psychosis. Gen Hosp Psychiatry 2012;34:436.e9-11.
    • (2012) Gen Hosp Psychiatry , vol.34 , pp. 436.e9-436.e11
    • Chuo, Y.P.1    Hou, P.H.2    Chan, C.H.3    Lin, C.C.4    Liao, Y.C.5
  • 12
    • 33745174181 scopus 로고    scopus 로고
    • Clinical characteristics of childhood-onset (juvenile) Huntington disease: Report of 12 patients and review of the literature
    • Gonzalez-Alegre P, Afifi AK. Clinical characteristics of childhood-onset (juvenile) Huntington disease: Report of 12 patients and review of the literature. J Child Neurol 2006;21:223-9.
    • (2006) J Child Neurol , vol.21 , pp. 223-229
    • Gonzalez-Alegre, P.1    Afifi, A.K.2
  • 13
    • 0030726155 scopus 로고    scopus 로고
    • Genetic testing of children at risk for Huntington’s disease. US Huntington Disease Genetic Testing Group
    • Nance MA. Genetic testing of children at risk for Huntington’s disease. US Huntington Disease Genetic Testing Group. Neurology 1997;49:1048-53.
    • (1997) Neurology , vol.49 , pp. 1048-1053
    • Nance, M.A.1
  • 16
    • 0028107864 scopus 로고
    • Mutation analysis in patients with possible but apparently sporadic Huntington’s disease
    • Davis MB, Bateman D, Quinn NP, Marsden CD, Harding AE. Mutation analysis in patients with possible but apparently sporadic Huntington’s disease. Lancet 1994;344:714-7.
    • (1994) Lancet , vol.344 , pp. 714-717
    • Davis, M.B.1    Bateman, D.2    Quinn, N.P.3    Marsden, C.D.4    Harding, A.E.5
  • 17
    • 84933532765 scopus 로고    scopus 로고
    • Clinical phenotype and genetic analysis of sporadic Huntington’s disease clinical phenotype and genetic analysis (in Chinese)
    • Wang YX, Zhang BS. Clinical phenotype and genetic analysis of sporadic Huntington’s disease clinical phenotype and genetic analysis (in Chinese). Tianjin Med J 2010;38:1006-7.
    • (2010) Tianjin Med J , vol.38 , pp. 1006-1007
    • Wang, Y.X.1    Zhang, B.S.2
  • 18
    • 0036626868 scopus 로고    scopus 로고
    • Homozygosity in Huntington’s disease: New ethical dilemma caused by molecular diagnosis
    • Alonso ME, Yescas P, Rasmussen A, Ochoa A, Macías R, Ruiz I, et al. Homozygosity in Huntington’s disease: New ethical dilemma caused by molecular diagnosis. Clin Genet 2002;61:437-42.
    • (2002) Clin Genet , vol.61 , pp. 437-442
    • Alonso, M.E.1    Yescas, P.2    Rasmussen, A.3    Ochoa, A.4    Macías, R.5    Ruiz, I.6
  • 19
    • 0028316870 scopus 로고
    • A worldwide study of the Huntington’s disease mutation. The sensitivity and specificity of measuring CAG repeats
    • Kremer B, Goldberg P, Andrew SE, Theilmann J, Telenius H, Zeisler J, et al. A worldwide study of the Huntington’s disease mutation. The sensitivity and specificity of measuring CAG repeats. N Engl J Med 1994;330:1401-6.
    • (1994) N Engl J Med , vol.330 , pp. 1401-1406
    • Kremer, B.1    Goldberg, P.2    Andrew, S.E.3    Theilmann, J.4    Telenius, H.5    Zeisler, J.6
  • 20
    • 84655161604 scopus 로고    scopus 로고
    • A Chinese pedigree with an individual homozygous for CAG repeats of Huntington’s disease
    • Shi SS, Lin Y, Zhao GX, Gan SR, Wu ZY. A Chinese pedigree with an individual homozygous for CAG repeats of Huntington’s disease. Psychiatr Genet 2012;22:53-4.
    • (2012) Psychiatr Genet , vol.22 , pp. 53-54
    • Shi, S.S.1    Lin, Y.2    Zhao, G.X.3    Gan, S.R.4    Wu, Z.Y.5
  • 21
    • 4644293999 scopus 로고    scopus 로고
    • DNA haplotype analysis of CAG repeat in Taiwanese Huntington’s disease patients
    • Wang CK, Wu YR, Hwu WL, Chen CM, Ro LS, Chen ST, et al. DNA haplotype analysis of CAG repeat in Taiwanese Huntington’s disease patients. Eur Neurol 2004;52:96-100.
    • (2004) Eur Neurol , vol.52 , pp. 96-100
    • Wang, C.K.1    Wu, Y.R.2    Hwu, W.L.3    Chen, C.M.4    Ro, L.S.5    Chen, S.T.6
  • 22
    • 0029338966 scopus 로고
    • A study on Huntington’s disease associated trinucleotide repeat within the Chinese population
    • Soong BW, Wang JT. A study on Huntington’s disease associated trinucleotide repeat within the Chinese population. Proc Natl Sci Counc Repub China B 1995;19:137-42.
    • (1995) Proc Natl Sci Counc Repub China B , vol.19 , pp. 137-142
    • Soong, B.W.1    Wang, J.T.2
  • 23
    • 0033812250 scopus 로고    scopus 로고
    • Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India
    • Pramanik S, Basu P, Gangopadhaya PK, Sinha KK, Jha DK, Sinha S, et al. Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India. Eur J Hum Genet 2000;8:678-82.
    • (2000) Eur J Hum Genet , vol.8 , pp. 678-682
    • Pramanik, S.1    Basu, P.2    Gangopadhaya, P.K.3    Sinha, K.K.4    Jha, D.K.5    Sinha, S.6
  • 24
    • 84892525250 scopus 로고    scopus 로고
    • CAG-expansion haplotype analysis in a population with a low prevalence of Huntington’s disease
    • Pulkes T, Papsing C, Wattanapokayakit S, Mahasirimongkol S. CAG-expansion haplotype analysis in a population with a low prevalence of Huntington’s disease. J Clin Neurol 2014;10:32-6.
    • (2014) J Clin Neurol , vol.10 , pp. 32-36
    • Pulkes, T.1    Papsing, C.2    Wattanapokayakit, S.3    Mahasirimongkol, S.4
  • 25
  • 26
    • 77349122826 scopus 로고    scopus 로고
    • CAG-repeat length and the age of onset in Huntington disease (HD): A review and validation study of statistical approaches
    • Langbehn DR, Hayden MR, Paulsen JS, PREDICT-HD Investigators of the Huntington Study Group. CAG-repeat length and the age of onset in Huntington disease (HD): A review and validation study of statistical approaches. Am J Med Genet B Neuropsychiatr Genet 2010;153B: 397-408.
    • (2010) Am J Med Genet B Neuropsychiatr Genet , vol.153B , pp. 397-408
    • Langbehn, D.R.1    Hayden, M.R.2    Paulsen, J.S.3
  • 27
    • 72249116078 scopus 로고    scopus 로고
    • Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease
    • Aziz NA, Jurgens CK, Landwehrmeyer GB, EHDN Registry Study Group, van Roon-Mom WM, van Ommen GJ, et al. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease. Neurology 2009;73:1280-5.
    • (2009) Neurology , vol.73 , pp. 1280-1285
    • Aziz, N.A.1    Jurgens, C.K.2    Landwehrmeyer, G.B.3    van Roon-Mom, W.M.4    van Ommen, G.J.5
  • 28
    • 84897918971 scopus 로고    scopus 로고
    • Huntingtin gene CAG repeat numbers in Chinese patients with Huntington’s disease and controls
    • Jiang H, Sun YM, Hao Y, Yan YP, Chen K, Xin SH, et al. Huntingtin gene CAG repeat numbers in Chinese patients with Huntington’s disease and controls. Eur J Neurol 2014;21:637-42.
    • (2014) Eur J Neurol , vol.21 , pp. 637-642
    • Jiang, H.1    Sun, Y.M.2    Hao, Y.3    Yan, Y.P.4    Chen, K.5    Xin, S.H.6
  • 29
    • 52649139552 scopus 로고    scopus 로고
    • The relationship between CAG repeat length and clinical progression in Huntington’s disease
    • Ravina B, Romer M, Constantinescu R, Biglan K, Brocht A, Kieburtz K, et al. The relationship between CAG repeat length and clinical progression in Huntington’s disease. Mov Disord 2008;23:1223-7.
    • (2008) Mov Disord , vol.23 , pp. 1223-1227
    • Ravina, B.1    Romer, M.2    Constantinescu, R.3    Biglan, K.4    Brocht, A.5    Kieburtz, K.6
  • 30
    • 61549104503 scopus 로고    scopus 로고
    • CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup
    • Warby SC, Montpetit A, Hayden AR, Carroll JB, Butland SL, Visscher H, et al. CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup. Am J Hum Genet 2009;84:351-66.
    • (2009) Am J Hum Genet , vol.84 , pp. 351-366
    • Warby, S.C.1    Montpetit, A.2    Hayden, A.R.3    Carroll, J.B.4    Butland, S.L.5    Visscher, H.6
  • 31
    • 79955758366 scopus 로고    scopus 로고
    • HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia
    • Warby SC, Visscher H, Collins JA, Doty CN, Carter C, Butland SL, et al. HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia. Eur J Hum Genet 2011;19:561-6.
    • (2011) Eur J Hum Genet , vol.19 , pp. 561-566
    • Warby, S.C.1    Visscher, H.2    Collins, J.A.3    Doty, C.N.4    Carter, C.5    Butland, S.L.6
  • 32
    • 0029015792 scopus 로고
    • Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes
    • Pêcheux C, Mouret JF, Dürr A, Agid Y, Feingold J, Brice A, et al. Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes. J Med Genet 1995;32:399-400.
    • (1995) J Med Genet , vol.32 , pp. 399-400
    • Pêcheux, C.1    Mouret, J.F.2    Dürr, A.3    Agid, Y.4    Feingold, J.5    Brice, A.6
  • 33
    • 77958154407 scopus 로고    scopus 로고
    • Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population
    • Ma M, Yang Y, Shang H, Su D, Zhang H, Ma Y, et al. Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population. J Neurol Sci 2010;298:57-60.
    • (2010) J Neurol Sci , vol.298 , pp. 57-60
    • Ma, M.1    Yang, Y.2    Shang, H.3    Su, D.4    Zhang, H.5    Ma, Y.6
  • 34
    • 84155164647 scopus 로고    scopus 로고
    • CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington’s disease in mainland Chinese families
    • Zhang BR, Tian J, Yan YP, Yin XZ, Zhao GH, Wu ZY, et al. CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington’s disease in mainland Chinese families. J Neurol Sci 2012;312:92-6.
    • (2012) J Neurol Sci , vol.312 , pp. 92-96
    • Zhang, B.R.1    Tian, J.2    Yan, Y.P.3    Yin, X.Z.4    Zhao, G.H.5    Wu, Z.Y.6
  • 35
    • 0029027047 scopus 로고
    • Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington’s disease
    • Masuda N, Goto J, Murayama N, Watanabe M, Kondo I, Kanazawa I. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington’s disease. J Med Genet 1995;32:701-5.
    • (1995) J Med Genet , vol.32 , pp. 701-705
    • Masuda, N.1    Goto, J.2    Murayama, N.3    Watanabe, M.4    Kondo, I.5    Kanazawa, I.6
  • 37
    • 84887547769 scopus 로고    scopus 로고
    • Onjisaponin B derived from radix polygalae enhances autophagy and accelerates the degradation of mutant a-synuclein and huntingtin in PC-12 cells
    • Wu AG, Wong VK, Xu SW, Chan WK, Ng CI, Liu L, et al. Onjisaponin B derived from radix polygalae enhances autophagy and accelerates the degradation of mutant a-synuclein and huntingtin in PC-12 cells. Int J Mol Sci 2013;14:22618-41.
    • (2013) Int J Mol Sci , vol.14 , pp. 22618-22641
    • Wu, A.G.1    Wong, V.K.2    Xu, S.W.3    Chan, W.K.4    Ng, C.I.5    Liu, L.6
  • 38
    • 84883819112 scopus 로고    scopus 로고
    • Huntington disease arises from a combinatory toxicity of polyglutamine and copper binding
    • Xiao G, Fan Q, Wang X, Zhou B. Huntington disease arises from a combinatory toxicity of polyglutamine and copper binding. Proc Natl Acad Sci U S A 2013;110:14995-5000.
    • (2013) Proc Natl Acad Sci U S A , vol.110 , pp. 14995-15000
    • Xiao, G.1    Fan, Q.2    Wang, X.3    Zhou, B.4
  • 39
    • 84933497538 scopus 로고    scopus 로고
    • Guideline for diagnosis and treatment of Huntington’s disease
    • Parkinson’s disease and movement disorder group in Neurologic Branch of Chinese Medical Association. Guideline for diagnosis and treatment of Huntington’s disease. Chin J Neurol 2011;44:638-41.
    • (2011) Chin J Neurol , vol.44 , pp. 638-641
  • 40
    • 84879137286 scopus 로고    scopus 로고
    • A systematic review of the intergenerational aspects and the diverse genetic profiles of Huntington’s disease
    • Agostinho LA, Dos Santos SR, Alvarenga RM, Paiva CL. A systematic review of the intergenerational aspects and the diverse genetic profiles of Huntington’s disease. Genet Mol Res 2013;12:1974-81.
    • (2013) Genet Mol Res , vol.12 , pp. 1974-1981
    • Agostinho, L.A.1    Dos Santos, S.R.2    Alvarenga, R.M.3    Paiva, C.L.4
  • 41
    • 70449931956 scopus 로고    scopus 로고
    • Motor abnormalities in premanifest persons with Huntington’s disease: The PREDICT-HD study
    • Biglan KM, Ross CA, Langbehn DR, Aylward EH, Stout JC, Queller S, et al. Motor abnormalities in premanifest persons with Huntington’s disease: The PREDICT-HD study. Mov Disord 2009;24:1763-72.
    • (2009) Mov Disord , vol.24 , pp. 1763-1772
    • Biglan, K.M.1    Ross, C.A.2    Langbehn, D.R.3    Aylward, E.H.4    Stout, J.C.5    Queller, S.6
  • 43
    • 83555173501 scopus 로고    scopus 로고
    • Potential endpoints for clinical trials in premanifest and early Huntington’s disease in the TRACK-HD study: Analysis of 24 month observational data
    • Tabrizi SJ, Reilmann R, Roos RA, Durr A, Leavitt B, Owen G, et al. Potential endpoints for clinical trials in premanifest and early Huntington’s disease in the TRACK-HD study: Analysis of 24 month observational data. Lancet Neurol 2012;11:42-53.
    • (2012) Lancet Neurol , vol.11 , pp. 42-53
    • Tabrizi, S.J.1    Reilmann, R.2    Roos, R.A.3    Durr, A.4    Leavitt, B.5    Owen, G.6
  • 46
    • 84891953394 scopus 로고    scopus 로고
    • Diffusion MRI measured white matter microstructure as a biomarker of neurodegeneration in preclinical Huntington’s disease
    • Kincses ZT, Szabó N, Tóth E, Zádori D, Faragó P, Németh D, et al. Diffusion MRI measured white matter microstructure as a biomarker of neurodegeneration in preclinical Huntington’s disease. Ideggyogy Sz 2013;66:399-405.
    • (2013) Ideggyogy Sz , vol.66 , pp. 399-405
    • Kincses, Z.T.1    Szabó, N.2    Tóth, E.3    Zádori, D.4    Faragó, P.5    Németh, D.6
  • 48
    • 77953894712 scopus 로고    scopus 로고
    • Huntington’s disease: Progress toward effective disease-modifying treatments and a cure
    • Johnson CD, Davidson BL. Huntington’s disease: Progress toward effective disease-modifying treatments and a cure. Hum Mol Genet 2010;19:R98-102.
    • (2010) Hum Mol Genet , vol.19 , pp. R98-R102
    • Johnson, C.D.1    Davidson, B.L.2
  • 49
    • 84865646926 scopus 로고    scopus 로고
    • Therapy in Huntington’s disease: Where are we?
    • Nance MA. Therapy in Huntington’s disease: Where are we? Curr Neurol Neurosci Rep 2012;12:359-66.
    • (2012) Curr Neurol Neurosci Rep , vol.12 , pp. 359-366
    • Nance, M.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.