Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
- Author(s)
- Rafehi, H; Green, C; Bozaoglu, K; Gillies, G; Delatycki, MB; Lockhart, PJ; Scheffer, IE; Bahlo, M;
- Journal Title
- European Journal of Human Genetics
- Publication Type
- epub ahead of print
- Abstract
- 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.
- Publisher
- NPG
- Research Division(s)
- Bioinformatics
- PubMed ID
- 35945246
- Publisher's Version
- https://doi.org/10.1038/s41431-022-01166-y
- Open Access at Publisher's Site
https://doi.org/10.1038/s41431-022-01166-y- NHMRC Grants
- NHMRC/GNT1102971, NHMRC/1194364, NHMRC/1032364, NHMRC/1006110, NHMRC/GNT1104831,
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- Refer to copyright notice on published article.
Creation Date: 2022-08-19 09:30:36
Last Modified: 2022-08-19 09:40:22