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PT  - JOURNAL ARTICLE
AU  - Katsube, T.
AU  - Shimono, T.
AU  - Ashikaga, R.
AU  - Hosono, M.
AU  - Kitagaki, H.
AU  - Murakami, T.
TI  - Demonstration of Cerebellar Atrophy in Neuroacanthocytosis of 2 Siblings
AID  - 10.3174/ajnr.A1282
DP  - 2009 Feb 01
TA  - American Journal of Neuroradiology
PG  - 386--388
VI  - 30
IP  - 2
4099  - http://www.ajnr.org/content/30/2/386.short
4100  - http://www.ajnr.org/content/30/2/386.full
SO  - Am. J. Neuroradiol.2009 Feb 01; 30
AB  - SUMMARY: Neuroacanthocytosis is a rare hereditary disorder characterized by involuntary choreiform movements and erythrocytic acanthocytosis in the peripheral blood. Clinical manifestations of this disorder resemble those of Huntington disease (HD). Neuroimaging features of neuroacanthocytosis are atrophy and signal intensity change of the striata on MR imaging, as in HD. We report herein the cases of 2 siblings with neuroacanthocytosis showing cerebellar atrophy as well as atrophy and signal intensity changes of striata.