Therapy in Huntington’s Disease: Where Are We?

被引:0
|
作者
Martha A. Nance
机构
[1] Struthers Parkinson’s Center,Huntington Disease Society of America Center of Excellence
[2] Hennepin County Medical Center,Department of Neurology
[3] University of Minnesota,undefined
来源
Current Neurology and Neuroscience Reports | 2012年 / 12卷
关键词
Huntington’s disease; Therapy; Tetrabenazine; Atypical antipsychotic; Amantadine; Selective serotonin reuptake inhibitor; Clonazepam; Physical therapy; Occupational therapy; Speech therapy; Dysphagia; Nutrition; Palliative care; Hospice;
D O I
暂无
中图分类号
学科分类号
摘要
As of 2012, almost 20 years after the discovery of the causative gene, clinical research has yet to find a disease-modifying treatment for Huntington’s disease. However, both pharmacologic and nonpharmacologic therapies are available for many of the common symptoms of the disease. Recent studies of gene-positive patients in the prodromal, not clinically diagnosable, stages of the disease, are changing our perception of when the process of neurodegeneration begins. Once disease-modifying therapies become available, the approach to the diagnosis of Huntington’s disease will likely shift from an examination-based clinical diagnosis, to one that includes a more complex combination of imaging, examination, and biomarker analysis.
引用
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页码:359 / 366
页数:7
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