Literature DB >> 22595899

Inherited cerebellar ataxia in childhood: a pattern-recognition approach using brain MRI.

L Vedolin1, G Gonzalez, C F Souza, C Lourenço, A J Barkovich.   

Abstract

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.

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Year:  2012        PMID: 22595899      PMCID: PMC7964648          DOI: 10.3174/ajnr.A3055

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  44 in total

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4.  The wobbly child: an approach to inherited ataxias.

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5.  Definition and classification of negative motor signs in childhood.

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6.  Cerebellar development in the preterm neonate: effect of supratentorial brain injury.

Authors:  Emily W Y Tam; Donna M Ferriero; Duan Xu; Jeffrey I Berman; Daniel B Vigneron; A James Barkovich; Steven P Miller
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7.  Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.

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Review 8.  Ataxias with autosomal, X-chromosomal or maternal inheritance.

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Journal:  Can J Neurol Sci       Date:  2009-07       Impact factor: 2.104

Review 9.  Abnormalities of cerebellar foliation and fissuration: classification, neurogenetics and clinicoradiological correlations.

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Journal:  Neuroradiology       Date:  2002-06-26       Impact factor: 2.804

Review 10.  Malformations of the midbrain and hindbrain: a retrospective study and review of the literature.

Authors:  Ozlem Alkan; Osman Kizilkilic; Tulin Yildirim
Journal:  Cerebellum       Date:  2009-04-01       Impact factor: 3.847

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Journal:  AJNR Am J Neuroradiol       Date:  2013-01-17       Impact factor: 3.825

3.  Reply: To PMID 23328073.

Authors:  L Vedolin
Journal:  AJNR Am J Neuroradiol       Date:  2013-02       Impact factor: 3.825

4.  Determination of Genotypic and Phenotypic Characteristics of Friedreich's Ataxia and Autosomal Dominant Spinocerebellar Ataxia Types 1, 2, 3, and 6.

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Review 5.  A case of McLeod phenotype of neuroacanthocytosis brain MR features and literature review.

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6.  Early Onset Ataxia with Comorbid Dystonia: Clinical, Anatomical and Biological Pathway Analysis Expose Shared Pathophysiology.

Authors:  Deborah A Sival; Martinica Garofalo; Rick Brandsma; Tom A Bokkers; Marloes van den Berg; Tom J de Koning; Marina A J Tijssen; Dineke S Verbeek
Journal:  Diagnostics (Basel)       Date:  2020-11-24

7.  Editorial: MRI-Based Methods for the Identification of Cerebellar Ataxia Types.

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Journal:  Front Neurosci       Date:  2022-02-16       Impact factor: 4.677

8.  Combined Genome, Transcriptome and Metabolome Analysis in the Diagnosis of Childhood Cerebellar Ataxia.

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  8 in total

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