Autonomic dysfunction in multiple system atrophy: from pathophysiology to clinical manifestations

Introduction Multiple system atrophy (MSA) is a sporadic, fatal, and rapidly progressive neurodegenerative disease of unknown etiology, pathologically characterized by the presence of α-synuclein (α-syn) immunoreactive cytoplasmic inclusions in oligodendrocytes. The deposition of α-synuclein in high...

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Principais autores:	Yuqi Luo, Nan Yang, Wanlin Yang, Baoling Chen, Shuzhen Zhu, YihRu Wu, Qing Wang
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Taylor & Francis Group 2025-12-01
coleção:	Annals of Medicine
Assuntos:	Multiple system atrophy central autonomic network autonomic dysfunction pathophysiology clinical manifestations
Acesso em linha:	https://www.tandfonline.com/doi/10.1080/07853890.2025.2488111
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