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

ReplyLetter

Reply:

L. Vedolin
American Journal of Neuroradiology February 2013, 34 (2) E23; DOI: https://doi.org/10.3174/ajnr.A3481
L. Vedolin
aNeuroradiology Section Hospital Moinhos de Vento Porto Alegre, Brazil
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We greatly appreciate Dr Mascalchi's interest in our article “Inherited Cerebellar Ataxia in Childhood: A Pattern-Recognition Approach Using Brain MRI.”1 We agree that many cases of Friedreich ataxia (FRDA) have normal MR imaging findings at the time of diagnosis and that a visually normal cerebellum in a child with ataxia usually suggests FRDA. We also concur that volume loss and decreased fractional anisotropy by diffusion tensor imaging of the superior cerebellar peduncles and iron deposition on T2* are potential biomarkers for this disease.2,3

References

  1. 1.
    1. Vedolin L,
    2. Gonzalez G,
    3. Souza CF,
    4. et al
    . Inherited cerebellar ataxia in childhood: a pattern-recognition approach using brain MRI. AJNR Am J Neuroradiol May 17 2012 [Epub ahead of print]
  2. 2.
    1. Della Nave R,
    2. Ginestroni A,
    3. Diciotti S,
    4. et al
    . Axial diffusivity is increased in the degenerating superior cerebellar peduncles of Friedreich's ataxia. Neuroradiology 2011;53:367–72
  3. 3.
    1. Koeppen AH,
    2. Michael SC,
    3. Knutson MD,
    4. et al
    . The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins. Acta Neuropathol 2007;114:163–73
  • © 2013 by American Journal of Neuroradiology
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