Neuroradiological Findings in the Spinocerebellar Ataxias

Background: The spinocerebellar ataxias (SCAs) are a group of autosomal dominant degenerative diseases characterized by cerebellar ataxia. Classified according to gene discovery, specific features of the SCAs – clinical, laboratorial, and neuroradiological (NR) – can facilitate establishing the diag...

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Veröffentlicht in:Tremor and other hyperkinetic movements (New York, N.Y.) N.Y.), 2019-09, Vol.9
Hauptverfasser: Meira, Alex Tiburtino, Arruda, Walter Oleschko, Ono, Sergio Eiji, De Carvalho Neto, Arnolfo, Raskin, Salmo, Camargo, Carlos Henrique F., Teive, Hélio Afonso G.
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Sprache:eng
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Zusammenfassung:Background: The spinocerebellar ataxias (SCAs) are a group of autosomal dominant degenerative diseases characterized by cerebellar ataxia. Classified according to gene discovery, specific features of the SCAs – clinical, laboratorial, and neuroradiological (NR) – can facilitate establishing the diagnosis. The purpose of this study was to review the particular NR abnormalities in the main SCAs.Methods: We conducted a literature search on this topic.Results: The main NR characteristics of brain imaging (magnetic resonance imaging or computerized tomography) in SCAs were: (1) pure cerebellar atrophy; (2) cerebellar atrophy with other findings (e.g., pontine, olivopontocerebellar, spinal, cortical, or subcortical atrophy; “hot cross bun sign”, and demyelinating lesions); (3) selective cerebellar atrophy; (4) no cerebellar atrophy.Discussion: The main NR abnormalities in the commonest SCAs, are not pathognomonic of any specific genotype, but can be helpful in limiting the diagnostic options. We are progressing to a better understanding of the SCAs, not only genetically, but also pathologically; NR is helpful in the challenge of diagnosing the specific genotype of SCA.
ISSN:2160-8288
2160-8288
DOI:10.5334/tohm.516