Marked asymmetry of putaminal pathology in an MSA‐P patient with Pisa syndrome | Zendy

Hozumi I. | Zendy; Piao Y.S. | Zendy; Inuzuka T. | Zendy; Matsuyama Z. | Zendy; Yamada Y. | Zendy; Hara A. | Zendy; Hirose T. | Zendy; Tsuchiya K. | Zendy; Takahashi H. | Zendy

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Marked asymmetry of putaminal pathology in an MSA‐P patient with Pisa syndrome

Author(s) -

Hozumi I.,

Piao Y.S.,

Inuzuka T.,

Matsuyama Z.,

Yamada Y.,

Hara A.,

Hirose T.,

Tsuchiya K.,

Takahashi H.

Publication year - 2004

Publication title -

movement disorders

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 3.352

H-Index - 198

eISSN - 1531-8257

pISSN - 0885-3185

DOI - 10.1002/mds.10668

Subject(s) - dystonia , atrophy , autopsy , pathophysiology , pathology , movement disorders , medicine , neurological disorder , psychology , pediatrics , central nervous system disease , neuroscience , disease

We report on an autopsy case of a 62‐year‐old Japanese woman with a 2.5‐year history of axial dystonia. She presented with a form of axial dystonia reminiscent of Pisa syndrome. The pathophysiological mechanism underlying forms of axial dystonia remains to be elucidated. We report here the histopathological findings of a multiple system atrophy of parkinsonian predominance (MSA‐P) patient with Pisa syndrome. © 2003 Movement Disorder Society

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