Subthalamic-thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor - A unusual clinical benefit

被引:54
|
作者
Freund, Hans-Joachim [1 ]
Barnikol, Utako B.
Nolte, Dagmar
Treuer, Harald
Auburger, Georg
Tass, Peter A.
Samii, Madjid
Sturm, Volker
机构
[1] Res Ctr Julich, Inst Neurosci & Biophys 3, D-52425 Julich, Germany
[2] Neuromodulat Res Ctr, Virtual Inst, Julich, Germany
[3] Int Neurosci Inst, Hannover, Germany
[4] Univ Cologne, Dept Stereotact & Funct Neurosurg, Cologne, Germany
[5] Univ Giessen, Inst Human Genet, Giessen, Germany
[6] Goethe Univ Frankfurt, Dept Neurol, Sect Mol Neurogenet, D-6000 Frankfurt, Germany
[7] Res Ctr Julich, Brain Imaging Ctr W, Julich, Germany
[8] Ctr Learning & Memory Res, Leibniz Inst Neurobiol, Magdeburg, Germany
关键词
deep brain stimulation; cerebellar tremor; long-lasting benefit; subthalamic target;
D O I
10.1002/mds.21338
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This is a single case report of a patient with spinocerebellar ataxia type 2 (SCA2) and severe tremor. Whereas disease progression with prevailing ataxia and dysmetria was slow over the first symptomatic 6 years, 6 months prior to operation were characterized by the development of a severe, debilitating postural tremor rendering the patient unable to independently sit, stand, speak, or swallow. Deep brain stimulation (DBS) at a subthalamic-thalamic electrode position almost completely arrested her tremor. The patient regained the functional state prior to her rapid disease progression allowing a restricted range of daily activities. Her condition has remained approximately stable over the two postoperative years to date. In addition to the efficacy of DBS on cerebellar tremor, the results illustrate a remarkable improvement of the patient's general condition and independence. (c) 2007 Movement Disorder Society.
引用
收藏
页码:732 / 735
页数:4
相关论文
共 50 条
  • [41] Clinical and genetic profile in index patients with spinocerebellar ataxia type 3 in Indonesia: case report
    Aminah, Siti
    Huda, Fathul
    Gamayani, Uni
    Pusparini, Iin
    Mochyadin, Mochammad Faisal Afif
    Sribudiani, Yunia
    Ibrahim, Norlinah Mohamed
    Achmad, Tri Hanggono
    HELIYON, 2021, 7 (07)
  • [42] Frequency and clinical phenotype of mutations in the gene for spinocerebellar ataxia type 2 (SCA2)
    Geschwind, D
    Perlman, S
    Pulst, SM
    NEUROLOGY, 1997, 48 (03) : 3076 - 3076
  • [43] Role of glutathione S-transferases in the spinocerebellar ataxia type 2 clinical phenotype
    Almaguer-Gotay, D.
    Almaguer-Mederos, L. E.
    Aguilera-Rodriguez, R.
    Estupinan-Rodriguez, A.
    Gonzalez-Zaldivar, Y.
    Cuello-Almarales, D.
    Laffita-Mesa, J. M.
    Vazquez-Mojena, Y.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2014, 341 (1-2) : 41 - 45
  • [44] Neurophysiological markers and their relationship with clinical and molecular parameters in the Cuban Spinocerebellar Ataxia Type 2
    Velazquez, LC
    Sanchez, G
    Garcia, JC
    Canales, N
    Almaguer, L
    Martinez, E
    MOVEMENT DISORDERS, 2004, 19 : S19 - S20
  • [45] Clinical and molecular analysis of a pedigree of southern Italian ancestry with spinocerebellar ataxia type 2
    Adams, C
    Starkman, S
    Pulst, SM
    NEUROLOGY, 1997, 49 (04) : 1163 - 1166
  • [46] Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report)
    Bouzid, Fatima Zahra
    Mansouri, Maria
    Abdelaziz, Chaikhy
    Louhab, Nisrine
    Bernard, Sablonniere
    Strubi-vuillaume, Isabelle
    Dafir, Kenza
    Aboussair, Nisrine
    PAN AFRICAN MEDICAL JOURNAL, 2021, 38
  • [47] Dysregulated Cerebrospinal Fluid Proteome of Spinocerebellar Ataxia Type 2 and its Clinical Implications
    Stezin, Albert
    Sathe, Gajanan J.
    Gajbhiye, Akshada
    Bharadwaj, Sujas
    Ghose, Vivek
    Bellad, Anikha
    Malo, Palash Kumar
    Holla, Vikram
    Hegde, Shantala
    Bharath, Rose Dawn
    Saini, Jitender
    Jain, Sanjeev
    Yadav, Ravi
    Pandey, Akhilesh
    Pal, Pramod Kumar
    MOVEMENT DISORDERS, 2024, 39 (08) : 1418 - 1423
  • [48] Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families
    A. Filla
    G. De Michele
    L. Santoro
    O. Calabrese
    I. Castaldo
    S. Giuffrida
    D. Restivo
    L. Serlenga
    D. F. Condorelli
    U. Bonuccelli
    R. Scala
    G. Coppola
    G. Caruso
    S. Cocozza
    Journal of Neurology, 1999, 246 : 467 - 471
  • [49] Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families
    Filla, A
    De Michele, G
    Santoro, L
    Calabrese, O
    Castaldo, I
    Giuffrida, S
    Restivo, D
    Serlenga, L
    Condorelli, DF
    Bonuccelli, U
    Scala, R
    Coppola, G
    Caruso, G
    Cocozza, S
    JOURNAL OF NEUROLOGY, 1999, 246 (06) : 467 - 471
  • [50] An aged patient with spinocerebellar ataxia type 2: an autopsy case report with review of the literature
    Ishida, C.
    Komai, K.
    Yonezawa, K.
    Sakajiri, K-, I
    Nitta, E.
    Kawashima, A.
    Yamada, M.
    BRAIN PATHOLOGY, 2010, 20 : 36 - 36