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Myoclonus in Ataxia–Telangiectasia

BACKGROUND: Various movement disorders can be found in ataxia–telangiectasia (AT), including ataxia, dystonia, chorea, and myoclonus, but myoclonus has rarely been described as the predominant feature in AT. CASE REPORT: We report two AT patients with prominent myoclonus, illustrating an unusual pre...

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Detalles Bibliográficos
Autores principales: Termsarasab, Pichet, Yang, Amy C., Frucht, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Columbia University Libraries/Information Services 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365056/
https://www.ncbi.nlm.nih.gov/pubmed/25793145
http://dx.doi.org/10.7916/D88P5Z9X
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author Termsarasab, Pichet
Yang, Amy C.
Frucht, Steven J.
author_facet Termsarasab, Pichet
Yang, Amy C.
Frucht, Steven J.
author_sort Termsarasab, Pichet
collection PubMed
description BACKGROUND: Various movement disorders can be found in ataxia–telangiectasia (AT), including ataxia, dystonia, chorea, and myoclonus, but myoclonus has rarely been described as the predominant feature in AT. CASE REPORT: We report two AT patients with prominent myoclonus, illustrating an unusual presentation of this disorder. Sequencing of the ATM gene in the first patient revealed a homozygous truncating mutation, c.5908C>T (p.Q1970*) in exon 38 of the ATM gene, which has been previously reported as a founder mutation in the Costa Rican population. DISCUSSION: Myoclonus can be a predominant or presenting feature in AT, even without dystonia.
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spelling pubmed-43650562015-03-19 Myoclonus in Ataxia–Telangiectasia Termsarasab, Pichet Yang, Amy C. Frucht, Steven J. Tremor Other Hyperkinet Mov (N Y) Case Reports BACKGROUND: Various movement disorders can be found in ataxia–telangiectasia (AT), including ataxia, dystonia, chorea, and myoclonus, but myoclonus has rarely been described as the predominant feature in AT. CASE REPORT: We report two AT patients with prominent myoclonus, illustrating an unusual presentation of this disorder. Sequencing of the ATM gene in the first patient revealed a homozygous truncating mutation, c.5908C>T (p.Q1970*) in exon 38 of the ATM gene, which has been previously reported as a founder mutation in the Costa Rican population. DISCUSSION: Myoclonus can be a predominant or presenting feature in AT, even without dystonia. Columbia University Libraries/Information Services 2015-03-13 /pmc/articles/PMC4365056/ /pubmed/25793145 http://dx.doi.org/10.7916/D88P5Z9X Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution–Noncommerical–No Derivatives License, which permits the user to copy, distribute, and transmit the work provided that the original author and source are credited; that no commercial use is made of the work; and that the work is not altered or transformed.
spellingShingle Case Reports
Termsarasab, Pichet
Yang, Amy C.
Frucht, Steven J.
Myoclonus in Ataxia–Telangiectasia
title Myoclonus in Ataxia–Telangiectasia
title_full Myoclonus in Ataxia–Telangiectasia
title_fullStr Myoclonus in Ataxia–Telangiectasia
title_full_unstemmed Myoclonus in Ataxia–Telangiectasia
title_short Myoclonus in Ataxia–Telangiectasia
title_sort myoclonus in ataxia–telangiectasia
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365056/
https://www.ncbi.nlm.nih.gov/pubmed/25793145
http://dx.doi.org/10.7916/D88P5Z9X
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AT yangamyc myoclonusinataxiatelangiectasia
AT fruchtstevenj myoclonusinataxiatelangiectasia