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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

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Inherited Cerebellar Ataxia in Childhood: A Pattern-Recognition Approach Using Brain MRI

L. Vedolin, G. Gonzalez, C.F. Souza, C. Lourenço and A.J. Barkovich
American Journal of Neuroradiology May 2013, 34 (5) 925-934; DOI: https://doi.org/10.3174/ajnr.A3055
L. Vedolin
aFrom the Neuroradiology Section (L.V.), Hospital Moinhos de Vento, Porto Alegre, Brazil
ePediatric Neuroradiology (L.V., G.G., A.J.B.), University of California, San Francisco, California.
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G. Gonzalez
bRadiology Department (G.G.), Hospital San Juan de Dios, Santiago, Chile
ePediatric Neuroradiology (L.V., G.G., A.J.B.), University of California, San Francisco, California.
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C.F. Souza
cGenetics Department (C.F.S.), Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil
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C. Lourenço
dGenetics Department (C.L.), Universidade de Sao Paulo, Ribeirao Preto, Brazil
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A.J. Barkovich
ePediatric Neuroradiology (L.V., G.G., A.J.B.), University of California, San Francisco, California.
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Abstract

SUMMARY: Ataxia is the principal symptom of many common neurologic diseases in childhood. Ataxias caused by dysfunction of the cerebellum occur in acute, intermittent, and progressive disorders. Most of the chronic progressive processes are secondary to degenerative and metabolic diseases. In addition, congenital malformation of the midbrain and hindbrain can also be present, with posterior fossa symptoms related to ataxia. Brain MR imaging is the most accurate imaging technique to investigate these patients, and imaging abnormalities include size, shape, and/or signal of the brain stem and/or cerebellum. Supratentorial and cord lesions are also common. This review will discuss a pattern-recognition approach to inherited cerebellar ataxia in childhood. The purpose is to provide a comprehensive discussion that ultimately could help neuroradiologists better manage this important topic in pediatric neurology.

ABBREVIATIONS:

AR
autosomal recessive
CAC
cerebellar ataxia in childhood
4H
hypomyelination with hypogonadotropic hypogonadism and hypodontia
JSRD
Joubert syndrome and related disorders
OPHN1
oligophrenin-1
  • © 2013 by American Journal of Neuroradiology

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American Journal of Neuroradiology: 34 (5)
American Journal of Neuroradiology
Vol. 34, Issue 5
1 May 2013
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Cite this article
L. Vedolin, G. Gonzalez, C.F. Souza, C. Lourenço, A.J. Barkovich
Inherited Cerebellar Ataxia in Childhood: A Pattern-Recognition Approach Using Brain MRI
American Journal of Neuroradiology May 2013, 34 (5) 925-934; DOI: 10.3174/ajnr.A3055

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Inherited Cerebellar Ataxia in Childhood: A Pattern-Recognition Approach Using Brain MRI
L. Vedolin, G. Gonzalez, C.F. Souza, C. Lourenço, A.J. Barkovich
American Journal of Neuroradiology May 2013, 34 (5) 925-934; DOI: 10.3174/ajnr.A3055
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