Spinal muscular atrophy: Clinical classification and disease heterogeneity

被引:161
|
作者
Russman, Barry S.
机构
[1] Shriners Hosp Children, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97201 USA
关键词
spinal muscular atrophy; anterior horn cell; SMN1; gene;
D O I
10.1177/0883073807305673
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The clinical classification of spinal muscular atrophy, caused by deletion of the survival motor neuron I gene (SMNI), is based on age at onset and maximum function achieved. Evidence suggests that maximum function achieved is more closely related to life expectancy than age at onset. Therefore, it is important to wait for a period before assigning a patient to I of 5 classes of the disorder. Several diseases result from degeneration of the anterior horn cell but are not caused by SMN1. The classification for these conditions is evolving. This article offers an attempt at organizing one's thinking about this disease group.
引用
收藏
页码:946 / 951
页数:6
相关论文
共 50 条
  • [1] Clinical trials in spinal muscular atrophy
    Darras, Basil T.
    Kang, Peter B.
    CURRENT OPINION IN PEDIATRICS, 2007, 19 (06) : 675 - 679
  • [2] Clinical manifestations of spinal muscular atrophy in adult patients
    Horak, T.
    Bednarik, J.
    Horakova, M.
    Botikova, D.
    Vohanka, S.
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 2020, 83 : S13 - S16
  • [3] Spinal Muscular Atrophy A (Now) Treatable Neurodegenerative Disease
    Fay, Alex
    PEDIATRIC CLINICS OF NORTH AMERICA, 2023, 70 (05) : 963 - 977
  • [4] Clinical features of spinal muscular atrophy in children
    Stanek, J.
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 2020, 83 : S8 - S12
  • [5] Clinical Outcome Measures in Spinal Muscular Atrophy
    Montes, Jacqueline
    Gordon, Andrew M.
    Pandya, Shree
    De Vivo, Darryl C.
    Kaufmann, Petra
    JOURNAL OF CHILD NEUROLOGY, 2009, 24 (08) : 968 - 978
  • [6] Perspectives on clinical trials in spinal muscular atrophy
    Swoboda, Kathryn J.
    Kissel, John T.
    Crawford, Thomas O.
    Bromberg, Mark B.
    Acsadi, Gyula
    D'Anjou, Guy
    Krosschell, Kristin J.
    Reyna, Sandra P.
    Schroth, Mary K.
    Scott, Charles B.
    Simard, Louise R.
    JOURNAL OF CHILD NEUROLOGY, 2007, 22 (08) : 957 - 966
  • [7] Clinical Characteristics of Cases with Spinal Muscular Atrophy
    Canpolat, Mehmet
    Bayram, Ayse Kacar
    Bahadir, Oguzhan
    Per, Huseyin
    Gumus, Hakan
    Dundar, Munis
    Kumandas, Sefer
    GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS, 2016, 14 (01): : 18 - 22
  • [8] Clinical and molecular diagnosis of spinal muscular atrophy
    Panigrahi, I
    Kesari, A
    Phadke, SR
    Mittal, B
    NEUROLOGY INDIA, 2002, 50 (02) : 117 - 122
  • [9] Spinal muscular atrophy - Clinical and genetic correlations
    Zerres, K
    Wirth, B
    RudnikSchoneborn, S
    NEUROMUSCULAR DISORDERS, 1997, 7 (03) : 202 - 207
  • [10] Genetics of spinal muscular atrophy
    Hedvicakova, P.
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 2020, 83 : S17 - S20