Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature

Author:

Namekawa Michito,Takiyama Yoshihisa,Honda Junko,Shimazaki Haruo,Sakoe Kumi,Nakano Imaharu

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

Reference38 articles.

1. Alexander WS: Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant. Brain. 1949, 72: 373-381. 10.1093/brain/72.3.373.

2. Johnson AB: Alexander disease. Neurodystrophies and Neurolipidoses. Edited by: Moser HW. 1996, Amsterdam, Elsevier Science, 22 (66): 701-710. Vinken PJ and Bruyn GW (series Editors): Handbook of Clinical Neurology

3. Quinlan RA, Brenner M, Goldman JE, Messing A: GFAP and its role in Alexander disease. Exp Cell Res. 2007, 313: 2077-2087. 10.1016/j.yexcr.2007.04.004.

4. Iwaki T, Iwaki A, Tateishi J, Sakaki Y, Goldman JE: αB-crystallin and 27-kd heat shock protein are regulated by stress conditions in the central nervous system and accumulate in Rosenthal fibers. Am J Pathol. 1993, 143: 487-495.

5. Riggs JE, Schochet SS, Nelson J: Asymptomatic adult Alexander's disease: Entity or nasological misconception?. Neurology. 1988, 38: 152-154.

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