Limb apraxia in corticobasal degeneration and progressive supranuclear palsy

被引:36
|
作者
Soliveri, P [1 ]
Piacentini, S [1 ]
Girotti, F [1 ]
机构
[1] Ist Nazl Neurol Carlo Besta, Dept Neurol, I-20133 Milan, Italy
关键词
D O I
10.1212/01.WNL.0000150732.92567.BA
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Corticobasal degeneration (CBD) and progressive supranuclear palsy (PSP) share pathologic features, and cortical and subcortical signs. Apraxia is frequently described in CBD and sometimes in PSP; however, it is difficult to distinguish ideomotor from limb-kinetic apraxia, and apraxia frequency is unclear. The authors set out to clarify the nature and frequency of apraxia in these diseases. Methods: The authors compared probable CBD and PSP patients, matched for motor disability, to healthy age-matched controls on cognitive tests and the De Renzi ideomotor apraxia test. Results: Cognitive impairment was similar, but more CBD (70.8%) than PSP (36%) patients had apraxia. CBD patients committed more apraxic errors of awkwardness and were more compromised on simple gestures; PSP patients committed more sequence errors. Conclusions: While progressive supranuclear palsy ( PSP) patients had ideomotor apraxia, the peculiar gesture compromise in corticobasal degeneration (CBD) suggests that limb-kinetic apraxia is dominant. In both illnesses, the movement production system of Roy and Square appears compromised: in CBD defective control of muscle activation seems likely, producing clumsy movements; in PSP, control of motor program activation appears defective, resulting in sequence errors and perseverations. The De Renzi test can reliably estimate apraxia frequency and may be used to distinguish limb-kinetic from ideomotor apraxia.
引用
收藏
页码:448 / 453
页数:6
相关论文
共 50 条
  • [31] Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options
    Lamb, Ruth
    Rohrer, Jonathan D.
    Lees, Andrew J.
    Morris, Huw R.
    CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2016, 18 (09)
  • [32] Key emerging issues in progressive supranuclear palsy and corticobasal degeneration
    Josephs, Keith A.
    JOURNAL OF NEUROLOGY, 2015, 262 (03) : 783 - 788
  • [33] Electrophysiological comparison between corticobasal degeneration and progressive supranuclear palsy
    Takeda, M
    Tachibana, H
    Okuda, B
    Kawabata, K
    Sugita, M
    CLINICAL NEUROLOGY AND NEUROSURGERY, 1998, 100 (02) : 94 - 98
  • [34] Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options
    Ruth Lamb
    Jonathan D. Rohrer
    Andrew J. Lees
    Huw R. Morris
    Current Treatment Options in Neurology, 2016, 18
  • [35] Sonographic discrimination of corticobasal degeneration vs progressive supranuclear palsy
    Walter, U
    Dressler, D
    Wolters, A
    Probst, T
    Grossmann, A
    Benecke, R
    NEUROLOGY, 2004, 63 (03) : 504 - 509
  • [37] Cerebral blood flow in corticobasal degeneration and progressive supranuclear palsy
    Okuda, B
    Tachibana, H
    Kawabata, K
    Takeda, M
    Sugita, M
    ALZHEIMER DISEASE & ASSOCIATED DISORDERS, 2000, 14 (01): : 46 - 52
  • [38] Progressive supranuclear palsy and corticobasal degeneration: Lumping versus splitting
    Scaravilli, T
    Tolosa, E
    Ferrer, I
    MOVEMENT DISORDERS, 2005, 20 : S21 - S28
  • [39] Are frontotemporal lobar degeneration, progressive supranuclear palsy and corticobasal degeneration distinct diseases?
    Sha, ron Sha
    Hou, Craig
    Viskontas, Indre V.
    Miller, Bruce L.
    NATURE CLINICAL PRACTICE NEUROLOGY, 2006, 2 (12): : 658 - 665
  • [40] Are frontotemporal lobar degeneration, progressive supranuclear palsy and corticobasal degeneration distinct diseases?
    Sharon Sha
    Craig Hou
    Indre V Viskontas
    Bruce L Miller
    Nature Clinical Practice Neurology, 2006, 2 : 658 - 665