Journal article
Cerebral abnormalities in Friedreich ataxia: A review
LP Selvadurai, IH Harding, LA Corben, N Georgiou-Karistianis
Neuroscience and Biobehavioral Reviews | PERGAMON-ELSEVIER SCIENCE LTD | Published : 2018
Abstract
Friedreich ataxia (FRDA) is an inherited degenerative disorder affecting multiple systems of the body and resulting in symptoms which include progressive ataxia, dysarthria, and cardiomyopathy. Central nervous system pathology has been traditionally ascribed to the spinal cord and dentate nucleus of the cerebellum. However, cerebral abnormalities in FRDA are being increasingly documented via multiple neuroimaging techniques. Understanding the nature and implications of cerebral abnormalities in FRDA provides more comprehensive knowledge of nervous system involvement in this disorder and increases the prospects of identifying effective treatment targets. We review the cerebellar and the cereb..
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Awarded by Friedreich's Ataxia Research Alliance
Funding Acknowledgements
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. IHH is supported by an Australian NHMRC Early Career Fellowship (ID: 1106533). LC receives funding from the Friedreich Ataxia Research Association (Australasia) and the Friedreich Ataxia Research Alliance (USA).