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Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing

Several neurological disorders, such as myotonic dystrophy are caused by expansions of short tandem repeats (STRs) which can be difficult to detect by molecular tools. Methodological advances have made repeat expansion (RE) detection with whole genome sequencing (WGS) feasible. We recruited a multi-...

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Autores principales: Rafehi, Haloom, Green, Cherie, Bozaoglu, Kiymet, Gillies, Greta, Delatycki, Martin B., Lockhart, Paul J., Scheffer, Ingrid E., Bahlo, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823003/
https://www.ncbi.nlm.nih.gov/pubmed/35945246
http://dx.doi.org/10.1038/s41431-022-01166-y
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author Rafehi, Haloom
Green, Cherie
Bozaoglu, Kiymet
Gillies, Greta
Delatycki, Martin B.
Lockhart, Paul J.
Scheffer, Ingrid E.
Bahlo, Melanie
author_facet Rafehi, Haloom
Green, Cherie
Bozaoglu, Kiymet
Gillies, Greta
Delatycki, Martin B.
Lockhart, Paul J.
Scheffer, Ingrid E.
Bahlo, Melanie
author_sort Rafehi, Haloom
collection PubMed
description Several neurological disorders, such as myotonic dystrophy are caused by expansions of short tandem repeats (STRs) which can be difficult to detect by molecular tools. Methodological advances have made repeat expansion (RE) detection with whole genome sequencing (WGS) feasible. We recruited a multi-generational family (family A) ascertained for genetic studies of autism spectrum disorder. WGS was performed on seven children from four nuclear families from family A and analyzed for REs of STRs known to cause neurological disorders. We detected an expansion of a heterozygous intronic CCTG STR in CNBP in two siblings. This STR causes myotonic dystrophy type 2 (DM2). The expansion did not segregate with the ASD phenotype. Repeat-primed PCR showed that the DM2 CCTG motif was expanded above the pathogenic threshold in both children and their mother. On subsequent examination, the mother had mild features of DM2. We show that screening of STRs in WGS datasets has diagnostic utility, both in the clinical and research domain, with potential management and genetic counseling implications.
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spelling pubmed-98230032023-01-08 Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing Rafehi, Haloom Green, Cherie Bozaoglu, Kiymet Gillies, Greta Delatycki, Martin B. Lockhart, Paul J. Scheffer, Ingrid E. Bahlo, Melanie Eur J Hum Genet Brief Communication Several neurological disorders, such as myotonic dystrophy are caused by expansions of short tandem repeats (STRs) which can be difficult to detect by molecular tools. Methodological advances have made repeat expansion (RE) detection with whole genome sequencing (WGS) feasible. We recruited a multi-generational family (family A) ascertained for genetic studies of autism spectrum disorder. WGS was performed on seven children from four nuclear families from family A and analyzed for REs of STRs known to cause neurological disorders. We detected an expansion of a heterozygous intronic CCTG STR in CNBP in two siblings. This STR causes myotonic dystrophy type 2 (DM2). The expansion did not segregate with the ASD phenotype. Repeat-primed PCR showed that the DM2 CCTG motif was expanded above the pathogenic threshold in both children and their mother. On subsequent examination, the mother had mild features of DM2. We show that screening of STRs in WGS datasets has diagnostic utility, both in the clinical and research domain, with potential management and genetic counseling implications. Springer International Publishing 2022-08-09 2023-01 /pmc/articles/PMC9823003/ /pubmed/35945246 http://dx.doi.org/10.1038/s41431-022-01166-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Brief Communication
Rafehi, Haloom
Green, Cherie
Bozaoglu, Kiymet
Gillies, Greta
Delatycki, Martin B.
Lockhart, Paul J.
Scheffer, Ingrid E.
Bahlo, Melanie
Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
title Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
title_full Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
title_fullStr Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
title_full_unstemmed Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
title_short Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
title_sort unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823003/
https://www.ncbi.nlm.nih.gov/pubmed/35945246
http://dx.doi.org/10.1038/s41431-022-01166-y
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