Adult-onset Alexander disease mimicking multiple system atrophy predominant cerebellar ataxia

被引：2
|
作者：
Watanabe, Yuji [1 ]
Tsukahara, Yuka [1 ]
Fujita, Hiroaki [1 ]
Sakuramoto, Hirotaka [1 ]
Shiina, Tomohiko [1 ]
Suzuki, Keisuke [1 ]
机构：
[1] Dokkyo Med Univ, Dept Neurol, 880 Kitakobayashi, Mibu, Tochigi 3210293, Japan
来源：
JOURNAL OF CLINICAL NEUROSCIENCE | 2021年 / 87卷
关键词：
Adult-onset Alexander disease; Multiple system atrophy; Dopamine transporter scan; MUTATION; FEATURES; GENE;
D O I：
10.1016/j.jocn.2021.03.001
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
[No abstract available]
引用
收藏
页码：150 / 152
页数：3
相关论文
共 50 条
  • [41] Superficial siderosis due to a lumbar ependymoma mimicking adult-onset spinocerebellar ataxia
    Spengos, Konstantinos
    Vassilopoulou, Sofia
    Tsivgoulis, Georgios
    Karachalios, Georgios
    Vassilopoulos, Demetris
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2007, 109 (08) : 705 - 707
  • [42] Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia
    Hiel, J. A. P.
    van Engelen, B. G. M.
    Weemaes, C. M. R.
    Broeks, A.
    Verrips, A.
    ter Laak, H.
    Vingerhoets, H. M.
    van den Heuvel, L. P. W.
    Lammens, M.
    Gabreels, F. J. M.
    Last, J. I.
    Taylor, A. M. R.
    NEUROLOGY, 2006, 67 (02) : 346 - 349
  • [43] Non-motor symptoms in Spinocerebellar ataxia, multiple system atrophy and Idiopathic late-onset cerebellar ataxia
    Park, Y. M.
    Kim, M. J.
    Koh, S. B.
    MOVEMENT DISORDERS, 2018, 33 : S281 - S281
  • [44] Very late-onset Friedreich's ataxia with minimal GAA1 expansion mimicking multiple system atrophy of cerebellar type
    Berciano, J
    Infante, J
    García, A
    Polo, JM
    Volpini, V
    Combarros, O
    JOURNAL OF NEUROLOGY, 2005, 252 : 30 - 31
  • [45] Very late-onset Friedreich's ataxia with minimal GAA1 expansion mimicking multiple system atrophy of cerebellar type
    Berciano, J
    Infante, J
    García, A
    Polo, JM
    Volpini, V
    Combarros, O
    MOVEMENT DISORDERS, 2005, 20 (12) : 1643 - 1645
  • [46] Familial Adult-Onset Alexander Disease with a Novel GFAP Mutation
    Ogura, Hana
    Maki, Futaba
    Sasaki, Naoshi
    Yoshida, Tomokatsu
    Hasegawa, Yasuhiro
    MOVEMENT DISORDERS CLINICAL PRACTICE, 2016, 3 (03): : 300 - 302
  • [47] Adult-onset Alexander disease with palatal myoclonus and intraventricular tumour
    Hirayama, T.
    Fukae, J.
    Noda, K.
    Fujishima, K.
    Yamamoto, T.
    Mori, K.
    Maeda, M.
    Hattori, N.
    Shiroma, N.
    Tsurui, S.
    Okuma, Y.
    EUROPEAN JOURNAL OF NEUROLOGY, 2008, 15 (02) : E16 - E17
  • [48] A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease
    Ciammola, Andrea
    Sangalli, Davide
    Sassone, Jenny
    Poletti, Barbara
    Carelli, Laura
    Banfi, Paolo
    Pappacoda, Gabriele
    Ceccherini, Isabella
    Grossi, Alice
    Maderna, Luca
    Pingue, Monica
    Girotti, Floriano
    Silani, Vincenzo
    FRONTIERS IN NEUROLOGY, 2019, 10
  • [49] Adult-onset Alexander disease with palatal tremor and intraventricular tumor
    Okuma, Y.
    Hirayama, T.
    Fukae, J.
    Noda, K.
    Fujishima, K.
    Hattori, N.
    MOVEMENT DISORDERS, 2007, 22 : S289 - S289
  • [50] Adult-onset Alexander disease: could facial myokymia be a symptom?
    Scola, Rosana Herminia
    Lorenzoni, Paulo J.
    Kay, Claudia S. K.
    Werneck, Lineu C.
    ARQUIVOS DE NEURO-PSIQUIATRIA, 2014, 72 (11) : 897 - 898
12345