进行性核上麻痹
共核细胞病
皮质基底变性
帕金森病
萎缩
医学
路易体
纯自主神经功能衰竭
自主神经失调
帕金森病
路易氏体型失智症
病理
心脏病学
直立生命体征
内科学
疾病
神经科学
心理学
痴呆
α-突触核蛋白
血压
作者
Shunsuke Koga,Ikuko Aiba
出处
期刊:PubMed
日期:2022-03-01
卷期号:74 (3): 257-262
标识
DOI:10.11477/mf.1416202021
摘要
Progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) are tauopathies that clinically present with atypical parkinsonism. Autonomic dysfunction is known to occur in synucleinopathies, particularly in cases of multiple system atrophy; however, the frequency and features of autonomic dysfunction in patients with tauopathies remain unclear. Recent studies have reported that urinary dysfunction and constipation are common and affect the prognosis of patients with PSP. In contrast, neurogenic orthostatic hypotension is rare in PSP, which is useful to distinguish PSP from multiple system atrophy and Lewy body disease. Urinary dysfunction is also commonly observed in patients with CBD and serves as an inclusion criterion for PSP syndrome in patients with CBD. However, this finding is not validated in other cohorts; therefore, further studies are warranted to confirm the usefulness of this criterion.
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