Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity

被引:24
|
作者
McCombe, P. A. [1 ,2 ]
Wray, N. R. [3 ]
Henderson, R. D. [1 ,2 ]
机构
[1] Univ Queensland, Clin Res Ctr, Brisbane, Qld, Australia
[2] Royal Brisbane & Womens Hosp, Dept Neurol, Brisbane, Qld, Australia
[3] Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
关键词
Amyotrophic lateral sclerosis; motor neuron disease; cognitive impairmemt; sensory disturbance; autonomic disturbance; FRONTOTEMPORAL LOBAR DEGENERATION; VALOSIN-CONTAINING PROTEIN; SPINAL MUSCULAR-ATROPHY; SOD1-G93A MOUSE MODEL; COGNITIVE IMPAIRMENT; SKELETAL-MUSCLE; NEURON DISEASE; TRANSGENIC MICE; BEHAVIORAL-CHANGES; C9ORF72; MUTATION;
D O I
10.1080/14737175.2017.1273772
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease defined by the presence of muscle weakness. The motor features of disease are heterogeneous in site of onset and progression. There are also extra-motor features in some patients. The genetic basis for extra-motor features is uncertain. The heterogeneity of ALS is an issue for clinical trials.Areas covered: This paper reviews the range and prevalence of extra-motor features associated with ALS, and highlights the current information about genetic associations with extra-motor features.Expert commentary: There are extra-motor features of ALS, but these are not found in all patients. The most common is cognitive abnormality. More data is required to ascertain whether extra-motor features arise with progression of disease. Extra-motor features are reported in patients with a range of causative genetic mutations, but are not found in all patients with these mutations. Further studies are required of the heterogeneity of ALS, and genotype/phenotype correlations are required, taking note of extra-motor features.
引用
收藏
页码:561 / 577
页数:17
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