Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation

被引：0
|
作者：
Antonio Orlacchio
Pasqua Montieri
Carla Babalini
Fabrizio Gaudiello
Giorgio Bernardi
Toshitaka Kawarai
机构：
[1] Centro Europeo di Ricerca sul Cervello (CERC),Laboratorio di Neurogenetica
[2] Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Santa Lucia,Dipartimento di Neuroscienze
[3] Università di Roma “Tor Vergata”,Department of Neurology
[4] Hyogo Brain and Heart Center,undefined
来源：
Journal of Neurology | 2011年 / 258卷
关键词：
Hereditary Spastic Paraplegia; Autosomal Dominant; Thin Corpus Callosum; Atypical Clinical Characteristic; Sphincter Incompetence;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：1361 / 1363
页数：2
相关论文
共 50 条
  • [41] Case report: Hereditary spastic paraplegia with thin corpus callosum
    Xhelili, Malbora
    Kuqo, Altin
    Reka, Eni
    Muharremi, Eti
    Rroji, Arben
    Kruja, Jera
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2021, 429 : 50 - 50
  • [42] Mutation analysis of the SPG11 gene in Italian patients with spastic paraplegia and thin corpus callosum
    Castellotti, B.
    Mariotti, C.
    Fancellu, R.
    Salsano, E.
    Castucci, A.
    Gellera, C.
    Pareyson, D.
    Taroni, F.
    JOURNAL OF NEUROLOGY, 2008, 255 : 65 - 65
  • [43] Case report: SPG11 hereditary spastic paraplegia with no thinning in the corpus callosum
    Alfaidi, N.
    Kurdi, K.
    Basindwah, A.
    Al Said, Y.
    Cupler, E.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2019, 405
  • [44] SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
    Namekawa, M
    Ribai, P
    Nelson, I
    Forlani, S
    Fellmann, F
    Goizet, C
    Depienne, C
    Stevanin, G
    Ruberg, M
    Dürr, A
    Brice, A
    NEUROLOGY, 2006, 66 (01) : 112 - 114
  • [45] SPG3A mutations are associated with pure and complex forms of Hereditary Spastic Paraplegia
    Claeys, Kristl
    Ivanova, Nevyana
    Deconinck, Tine
    Litvinenko, Ivan
    Jordanova, Albena
    Loefgren, Ann
    Nelis, Eva
    Mercelis, Rudy
    Auer-Grumbach, Michaela
    Priller, Josef
    Ceulemans, Berten
    Sereda, Michael
    Kremensky, Ivo
    Mitev, Vanio
    De Jonghe, Peter
    NEUROMUSCULAR DISORDERS, 2006, 16 : S63 - S63
  • [46] Quantitative analysis of speech diadochokinetic rate in hereditary spastic paraplegia SPG3A
    Agrimaki, V.
    Siriopoulou, S.
    Papanicolaou, E. Zamba
    Christodoulou, K.
    Konstantopoulos, K.
    MOVEMENT DISORDERS, 2023, 38 : S812 - S813
  • [47] Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset
    Brockmann, K
    Simpson, MA
    Faber, A
    Bönnernann, C
    Crosby, AH
    Gärtner, J
    NEUROPEDIATRICS, 2005, 36 (04) : 274 - 278
  • [48] Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum
    Franca, Marcondes C., Jr.
    D'Abreu, Anelyssa
    Maurer-Morelli, Claudia V.
    Seccolin, Rodrigo
    Appenzeller, Simone
    Alessio, Andreia
    Damasceno, Benito P.
    Nucci, Anamarli
    Cendes, Fernando
    Lopes-Cendes, Iscia
    MOVEMENT DISORDERS, 2007, 22 (11) : 1556 - 1562
  • [49] Hereditary spastic paraplegia with a thin corpus callosum and thalamic involvement in Japan
    Ueda, M
    Katayama, Y
    Kamiya, T
    Mishina, M
    Igarashi, H
    Okubo, S
    Senda, M
    Iwabuchi, K
    Terashi, A
    NEUROLOGY, 1998, 51 (06) : 1751 - 1754
  • [50] Peripheral nerve abnormalities in hereditary spastic paraplegia with thin corpus callosum
    Franca, M. C., Jr.
    d'Abreu, A.
    Nucci, A.
    Lopes-Cendes, I.
    NEUROMUSCULAR DISORDERS, 2006, 16 (9-10) : 649 - 649
12345