The Wilson films - Huntington's Chorea

被引:0
作者
Klein, Christine [1 ]
机构
[1] Univ Lubeck, Dept Neurol, Sect Clin & Mol Neurogenet, D-23562 Lubeck, Germany
关键词
Huntington's disease; chorea; trinucleotide repeat expansion; genetic testing; historic Queen Square video; DISEASE;
D O I
10.1002/mds.23986
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Wilson's Queen Square Case 9 with Huntington's chorea shows a 68-year-old man with mild to moderate generalized chorea, impaired fixation, and probable cognitive decline in keeping with a diagnosis of Huntington's disease (HD). An age of onset in the late sixties and a negative family history suggest a relatively small expanded trinucleotide repeat in the HTT gene in the patient and reduced penetrance of an even shorter repeat allele in one of his parents. A highly sensitive and specific gene test has been offered worldwide for diagnostic testing of HD for almost two decades. This test, obviously unavailable at Wilson's times, became the historic frontrunner for guidelines of symptomatic, presymptomatic, and prenatal testing for an adult-onset neurodegenerative disorder. Regarding treatment of HD, however, we are still awaiting the successful translation of research results into the development of effective cause-directed, neuropreventive and neurorestaurative therapies. (c) 2011 Movement Disorder Society
引用
收藏
页码:2464 / 2466
页数:3
相关论文
共 16 条
[11]  
Paulson HL, 2011, NEUROBIOLOGY HUNTING, P1
[12]  
Schneider S, SEM NEUROL IN PRESS
[13]   The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test [J].
Schneider, Susanne A. ;
Walker, Ruth H. ;
Bhatia, Kailash P. .
NATURE CLINICAL PRACTICE NEUROLOGY, 2007, 3 (09) :517-525
[14]   Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population [J].
Sequeiros, J. ;
Ramos, E. M. ;
Cerqueira, J. ;
Costa, M. C. ;
Sousa, A. ;
Pinto-Basto, J. ;
Alonso, I. .
CLINICAL GENETICS, 2010, 78 (04) :381-387
[15]   Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis [J].
Tabrizi, Sarah J. ;
Scahill, Rachael I. ;
Durr, Alexandra ;
Roos, Raymund A. C. ;
Leavitt, Blair R. ;
Jones, Rebecca ;
Landwehrmeyer, G. Bernhard ;
Fox, Nick C. ;
Johnson, Hans ;
Hicks, Stephen L. ;
Kennard, Christopher ;
Craufurd, David ;
Frost, Chris ;
Langbehn, Douglas R. ;
Reilmann, Ralf ;
Stout, Julie C. .
LANCET NEUROLOGY, 2011, 10 (01) :31-42
[16]   HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia [J].
Warby, Simon C. ;
Visscher, Henk ;
Collins, Jennifer A. ;
Doty, Crystal N. ;
Carter, Catherine ;
Butland, Stefanie L. ;
Hayden, Anna R. ;
Kanazawa, Ichiro ;
Ross, Colin J. ;
Hayden, Michael R. .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (05) :561-566