Spinal muscular atrophy: Clinical classification and disease heterogeneity

被引:165
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 46 条
[21]  
HAUSMANOWAPETRUSEWICZ I, 1985, J MED GENET, V22, P350, DOI 10.1136/jmg.22.5.350
[22]  
Hoffmann J., 1893, DEUT ZEITSCH NERVENH, V3, P427, DOI [10.10007/BF, DOI 10.1007/BF01668496]
[23]   PROSPECTIVE-STUDY OF SPINAL MUSCULAR-ATROPHY BEFORE AGE-6 YEARS [J].
IANNACCONE, ST ;
BROWNE, RH ;
SAMAHA, FJ ;
BUNCHER, CR .
PEDIATRIC NEUROLOGY, 1993, 9 (03) :187-193
[24]   Molecular genetics of distal hereditary motor neuropathies [J].
Irobi, J ;
De Jonghe, P ;
Timmerman, V .
HUMAN MOLECULAR GENETICS, 2004, 13 :R195-R202
[25]   Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31 [J].
Isozumi, K ;
DeLong, R ;
Kaplan, J ;
Deng, HX ;
Iqbal, Z ;
Hung, WY ;
Wilhelmsen, KC ;
Hentati, A ;
PericakVance, MA ;
Siddique, T .
HUMAN MOLECULAR GENETICS, 1996, 5 (09) :1377-1382
[26]   JUVENILE SPINAL MUSCULAR-ATROPHY - A NEW HEXOSAMINIDASE DEFICIENCY PHENOTYPE [J].
JOHNSON, WG ;
WIGGER, HJ ;
KARP, HR ;
GLAUBIGER, LM ;
ROWLAND, LP .
ANNALS OF NEUROLOGY, 1982, 11 (01) :11-16
[27]   HEXOSAMINIDASE-A DEFICIENCY MANIFESTING AS SPINAL MUSCULAR-ATROPHY OF LATE ONSET [J].
KARNI, A ;
NAVON, R ;
SADEH, M .
ANNALS OF NEUROLOGY, 1988, 24 (03) :451-453
[28]  
Kelly TE, 1999, AM J MED GENET, V87, P65, DOI 10.1002/(SICI)1096-8628(19991105)87:1<65::AID-AJMG13>3.0.CO
[29]  
2-5
[30]   Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region [J].
Korinthenberg, R ;
Sauer, M ;
Ketelsen, UP ;
Hanemann, CO ;
Stoll, G ;
Graf, M ;
Baborie, A ;
Volk, B ;
Wirth, B ;
RudnikSchoneborn, S ;
Zerres, K .
ANNALS OF NEUROLOGY, 1997, 42 (03) :364-368