Complicated hereditary spastic paraplegia with thin corpus callosum: Variation of phenotypic expression over time

被引:0
作者
Anne-Dörte Sperfeld
Jan Kassubek
Andrew H. Crosby
Beate Winner
Albert C. Ludolph
Ingo Uttner
C. Oliver Hanemann
机构
[1] University of Ulm,Dept. of Neurology
[2] St. George’s Hospital Medical School,Dept. of Medical Genetics
[3] University of London,undefined
[4] Dept. of Neurology,undefined
来源
Journal of Neurology | 2004年 / 251卷
关键词
Corpus Callosum; Paraplegia; Phenotypic Expression; Hereditary Spastic Paraplegia; Thin Corpus Callosum;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:1285 / 1287
页数:2
相关论文
共 50 条
  • [21] Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI
    Steffi Dreha-Kulaczewski
    Peter Dechent
    Gunther Helms
    Jens Frahm
    Jutta Gärtner
    Knut Brockmann
    Neuroradiology, 2006, 48 : 893 - 898
  • [22] Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI
    Dreha-Kulaczewski, Steffi
    Dechent, Peter
    Helms, Gunther
    Frahm, Jens
    Gaertner, Jutta
    Brockmann, Knut
    NEURORADIOLOGY, 2006, 48 (12) : 893 - 898
  • [23] Further clinical and genetic characterization of SPG11:: Hereditary spastic paraplegia with thin corpus callosum
    Olmez, A.
    Uyanik, G.
    Ozgul, R. K.
    Gross, C.
    Cirak, S.
    Elibol, B.
    Anlar, B.
    Winner, B.
    Hehr, U.
    Topaloglu, H.
    Winkler, J.
    NEUROPEDIATRICS, 2006, 37 (02) : 59 - 66
  • [24] Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation
    Antonio Orlacchio
    Pasqua Montieri
    Carla Babalini
    Fabrizio Gaudiello
    Giorgio Bernardi
    Toshitaka Kawarai
    Journal of Neurology, 2011, 258 : 1361 - 1363
  • [25] FAMILIAL SPASTIC PARAPLEGIA WITH MENTAL IMPAIRMENT AND THIN CORPUS-CALLOSUM
    NAKAMURA, A
    IZUMI, K
    UMEHARA, F
    KURIYAMA, M
    HOKEZU, Y
    NAKAGAWA, M
    SHIMMYOZU, K
    IZUMO, S
    OSAME, M
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1995, 131 (01) : 35 - 42
  • [26] Cognitive Profile in Spastic Paraplegia with Thin Corpus Callosum and Mutations in SPG11
    Siri, L.
    Battaglia, F. M.
    Tessa, A.
    Rossi, A.
    Di Rocco, M.
    Facchinetti, S.
    Mascaretti, M.
    Santorelli, F. M.
    Veneselli, E.
    Biancheri, R.
    NEUROPEDIATRICS, 2010, 41 (01) : 35 - 38
  • [27] Novel compound heterozygous mutations of the SPG11 gene in Korean families with hereditary spastic paraplegia with thin corpus callosum
    Sung-Min Kim
    Jeong-Seon Lee
    Suhyun Kim
    Hyun-Jung Kim
    Man-Ho Kim
    Kyoung-Min Lee
    Yoon-Ho Hong
    Kyung Seok Park
    Jung-Joon Sung
    Kwang-Woo Lee
    Journal of Neurology, 2009, 256 : 1714 - 1718
  • [28] SPG11 Mutations Cause Kjellin Syndrome, a Hereditary Spastic Paraplegia With Thin Corpus Callosum and Central Retinal Degeneration
    Orlen, Hanna
    Melberg, Atle
    Raininko, Raili
    Kumlien, Eva
    Entesarian, Miriam
    Soderberg, Per
    Pahlman, Magnus
    Darin, Niklas
    Kyllerman, Marten
    Holmberg, Eva
    Engler, Henry
    Eriksson, Urban
    Dahl, Niklas
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2009, 150B (07) : 984 - 992
  • [29] Novel compound heterozygous mutations of the SPG11 gene in Korean families with hereditary spastic paraplegia with thin corpus callosum
    Kim, Sung-Min
    Lee, Jeong-Seon
    Kim, Suhyun
    Kim, Hyun-Jung
    Kim, Man-Ho
    Lee, Kyoung-Min
    Hong, Yoon-Ho
    Park, Kyung Seok
    Sung, Jung-Joon
    Lee, Kwang-Woo
    JOURNAL OF NEUROLOGY, 2009, 256 (10) : 1714 - 1718
  • [30] Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11
    Rajakulendran, Sanjeev
    Paisan-Ruiz, Coro
    Houlden, Henry
    JOURNAL OF CLINICAL NEUROLOGY, 2011, 7 (02): : 102 - 104