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Review
. 2017 Apr 7:4:4.
doi: 10.1186/s40673-017-0062-x. eCollection 2017.

Friedreich Ataxia: current status and future prospects

Affiliations
Review

Friedreich Ataxia: current status and future prospects

Katrin Bürk. Cerebellum Ataxias. .

Abstract

Friedreich ataxia (FA) represents the most frequent type of inherited ataxia. Most patients carry homozygous GAA expansions in the first intron of the frataxin gene on chromosome 9. Due to epigenetic alterations, frataxin expression is significantly reduced. Frataxin is a mitochondrial protein. Its deficiency leads to mitochondrial iron overload, defective energy supply and generation of reactive oxygen species. This review gives an overview over clinical and genetic aspects of FA and discusses current concepts of frataxin biogenesis and function as well as new therapeutic strategies.

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References

    1. Friedreich N. Über degenerative Atrophie der spinalen Hinterstränge (On degenerative atrophy of the spinal dorsal columns) Virchows Arch Pathol Anat Physiol Klin Med. 1863;26:391–419. doi: 10.1007/BF01930976. - DOI
    1. Marie P. Sur l’hérédo-ataxie cérébelleuse. Sem Med. 1893;13:444–7.
    1. Vankan P. Prevalence gradients of Friedreich’s ataxia and R1b haplotype in Europe co-localize, suggesting a common Palaeolithic origin in the Franco-Cantabrian ice age refuge. J Neurochem. 2013;126(Suppl 1):11–20. doi: 10.1111/jnc.12215. - DOI - PubMed
    1. Dürr A, Cossee M, Agid Y, et al. Clinical and genetic abnormalities in patients with Friedreich’s ataxia. N Engl J Med. 1996;335(16):1169–75. doi: 10.1056/NEJM199610173351601. - DOI - PubMed
    1. Harding AE. Friedreich’s ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features. Brain. 1981;104(3):589–620. doi: 10.1093/brain/104.3.589. - DOI - PubMed