共 64 条
Nonmotor symptoms in sporadic versus familial forms of Parkinson's disease
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作者:

Chao, Yin Xia
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h-index: 0
机构:
Nat Neurosci Inst, Singapore 308433, Singapore
Duke Natl Univ Singapore Grad Med Sch, Singapore 169857, Singapore Nat Neurosci Inst, Singapore 308433, Singapore

Chew, Lai Mun
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h-index: 0
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Nat Neurosci Inst, Singapore 308433, Singapore
Singapore Gen Hosp, Dept Neurol, Singapore 169608, Singapore Nat Neurosci Inst, Singapore 308433, Singapore

Deng, Xiao
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h-index: 0
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Nat Neurosci Inst, Singapore 308433, Singapore
Singapore Gen Hosp, Dept Neurol, Singapore 169608, Singapore Nat Neurosci Inst, Singapore 308433, Singapore

Tan, Eng-King
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h-index: 0
机构:
Nat Neurosci Inst, Singapore 308433, Singapore
Duke Natl Univ Singapore Grad Med Sch, Singapore 169857, Singapore
Singapore Gen Hosp, Dept Neurol, Singapore 169608, Singapore Nat Neurosci Inst, Singapore 308433, Singapore
机构:
[1] Nat Neurosci Inst, Singapore 308433, Singapore
[2] Duke Natl Univ Singapore Grad Med Sch, Singapore 169857, Singapore
[3] Singapore Gen Hosp, Dept Neurol, Singapore 169608, Singapore
基金:
英国医学研究理事会;
关键词:
clinical symptoms;
genetic background;
Parkinson's disease;
pathophysiology;
management;
D O I:
10.2217/NMT.14.57
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Besides the classical motor symptoms, Parkinson's disease (PD) patients experience a wide range of nonmotor symptoms (NMS) throughout the disease course. However, due to the lack of recognition and understanding of the pathogenesis, NMS symptoms may be overlooked. Familial PD is a well-defined group that can provide a good model to investigate the mechanisms for both motor and NMS in PD. Some studies suggest that the frequency of NMS is not different between genetic and sporadic form of PD while others suggest that specific domains (such as neuropsychiatric symptoms) are more common in the genetic form. Early recognition of NMS may facilitate early diagnosis and monitoring of both sporadic and genetic PD.
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页码:147 / 153
页数:7
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