Spinocerebellar ataxia type 2 presenting with rapidly progressing muscle weakness and muscular atrophy

Geriatr Gerontol Int. 2018 Feb;18(2):361-364. doi: 10.1111/ggi.13206.

Authors

Satoru Morimoto¹, Masaki Takao², Yasushi Nishina¹, Keita Sakurai³, Tadashi Komiya⁴, Kazutomi Kanemaru¹, Shigeo Murayama¹

Affiliations

¹ Department of Neurology, Tokyo Metropolitan Geriatric Hospital and Institution of Gerontology, Tokyo, Japan.
² Department of Neurology and Stroke, Saitama Medical University International Medical Center, Saitama, Japan.
³ Department of Neurology, National Hospital Organization Tokyo National Hospital, Tokyo, Japan.
⁴ Department of Radiology, Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Tokyo, Japan.

PMID: 29461011
DOI: 10.1111/ggi.13206

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Disease Progression
Humans
Male
Middle Aged
Muscle Weakness / etiology
Muscular Atrophy / etiology
Spinocerebellar Ataxias / complications
Spinocerebellar Ataxias / diagnosis*
Time Factors