Young-onset sporadic amyotrophic lateral sclerosis: A distinct nosological entity?

被引:34
|
作者
Gouveia, Liliana Olim
de Carvalho, Mamede
机构
[1] Hosp Santa Maria, Dept Neurol, P-1649 Lisbon, Portugal
[2] Fac Med, Inst Mol Med, Neuromuscular Unit, Lisbon, Portugal
来源
AMYOTROPHIC LATERAL SCLEROSIS | 2007年 / 8卷 / 06期
关键词
amyotrophic lateral sclerosis; juvenile onset; sporadic; review of the literature;
D O I
10.1080/17482960701553956
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
There are few reports describing young-onset amyotrophic lateral sclerosis (ALS). Age at onset is a prognostic factor in ALS, and thus it is relevant to investigate the clinical features of very young ALS patients. We describe three young-onset ALS cases and review the literature. SOD1 mutations were not identified. Our cases and 24 others from the literature indicate that young-onset ALS is characterized by slowly progressive symmetrical weakness; nevertheless, progression is variable. Young-onset ALS seems to be a distinct clinical syndrome but its aetiological background is largely unknown.
引用
收藏
页码:323 / 327
页数:5
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