INTRAFAMILIAL HETEROGENEITY IN HEREDITARY MOTOR-NEURON DISEASE

被引:45
作者
APPELBAUM, JS
ROOS, RP
SALAZARGRUESO, EF
BUCHMAN, A
IANNACCONE, S
GLANTZ, R
SIDDIQUE, T
MASELLI, R
机构
[1] UNIV CHICAGO, MED CTR, DEPT NEUROL, MC2030, 5841 S MARYLAND AVE, CHICAGO, IL 60637 USA
[2] RUSH PRESBYTERIAN ST LUKES MED CTR, DEPT NEUROL, CHICAGO, IL 60612 USA
[3] TEXAS SCOTTISH RITE HOSP CRIPPLED CHILDREN, DEPT NEUROL, DALLAS, TX USA
[4] UNIV TEXAS SW, DALLAS, TX USA
[5] UNIV CALIF DAVIS, DEPT NEUROL, DAVIS, CA 95616 USA
[6] NORTHWESTERN UNIV, SCH MED, DEPT NEUROL, CHICAGO, IL 60611 USA
关键词
D O I
10.1212/WNL.42.8.1488
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Although there are varied inheritance patterns in motor neuron disease (MND), the phenotype of MND is reported to be constant within these families, ie, cases of amyotrophic lateral sclerosis or primary lateral sclerosis do not occur in pedigrees with cases of spinal muscular atrophy. We describe four pedigrees whose members diverged in the phenotype of MND expressed. The intrafamilial variation of phenotype suggests a similar pathogenesis for some of the varied types of familial MND and the need for careful inquiry of family history in all patients with MND.
引用
收藏
页码:1488 / 1492
页数:5
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