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Background <p>Most of fetal cardiac rhabdomyomas (CRs) are associated with tuberous sclerosis (TSC), an autosomal dominant inherited disorder caused by mutations in the <i>TSC1</i> or <i>TSC2</i> genes.</p> Methods <p>In this study, 12 fetuses with sonographically identified CR were included. A comprehensive analysis integrating prenatal echocardiographic findings, parental phenotypic characteristics, and genetic profiles of fetuses with CR were conducted. Karyotype and SNP-array/CNV-seq were performed simultaneously with Trio-WES.</p> Results <p>All CRs were observed in the ventricle, interventricular septum, and the atrium, while the left ventricle were the most common areas. All subjects did not detect arrhythmia during pregnancy. Beside CRs, irregular low echo in the brain was detected in Case 12. <i>TSC1</i> and <i>TSC2</i> variants were identified in all 12 fetuses (100%). Mutants of <i>TSC1</i> account for 25% (3/12) and <i>TSC2</i> account for 75%(9/12). Two-thirds of these variants were de novo. The P/LP variant spectrums in <i>TSC1</i>/<i>TSC2</i> includes 4 (34%) nonsense, 4 (33%) missense, 2 (17%) frameshift, 1 (8%) splice and 1 (8%) small deletion. A 780&#xa0;kb deletion in 9q34.13 (arr[hg19] 9q34.13 (132286422–133062068) × 1) encompassing the entire of <i>TSC1</i> gene, and the other two de novo mutants of c.1687G &gt; C and c.1106delT in <i>TSC2</i> gene had not been reported previously.</p> Conclusion <p>Combination of fetal CR detected by ultrasound and genetic testing can effectively diagnose the prenatal cases of TSC. Three novel variants in <i>TSC</i> genes enlarge the variants spectrum of <i>TSC</i>.</p>

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Whole exome sequencing in fetal cardiac rhabdomyoma detected by ultrasonography: an analysis of 12 cases

  • 期刊论文

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  • 发表日期：

    2025年11月24日

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  • Jing Liu,
  • Jun He,
  • Wanglan Tang,
  • Jing Chen,
  • Yingchun Luo,
  • Haoxian Li,
  • Zhuo Li,
  • Lingqian Wu

摘要

Background

Most of fetal cardiac rhabdomyomas (CRs) are associated with tuberous sclerosis (TSC), an autosomal dominant inherited disorder caused by mutations in the TSC1 or TSC2 genes.

Methods

In this study, 12 fetuses with sonographically identified CR were included. A comprehensive analysis integrating prenatal echocardiographic findings, parental phenotypic characteristics, and genetic profiles of fetuses with CR were conducted. Karyotype and SNP-array/CNV-seq were performed simultaneously with Trio-WES.

Results

All CRs were observed in the ventricle, interventricular septum, and the atrium, while the left ventricle were the most common areas. All subjects did not detect arrhythmia during pregnancy. Beside CRs, irregular low echo in the brain was detected in Case 12. TSC1 and TSC2 variants were identified in all 12 fetuses (100%). Mutants of TSC1 account for 25% (3/12) and TSC2 account for 75%(9/12). Two-thirds of these variants were de novo. The P/LP variant spectrums in TSC1/TSC2 includes 4 (34%) nonsense, 4 (33%) missense, 2 (17%) frameshift, 1 (8%) splice and 1 (8%) small deletion. A 780 kb deletion in 9q34.13 (arr[hg19] 9q34.13 (132286422–133062068) × 1) encompassing the entire of TSC1 gene, and the other two de novo mutants of c.1687G > C and c.1106delT in TSC2 gene had not been reported previously.

Conclusion

Combination of fetal CR detected by ultrasound and genetic testing can effectively diagnose the prenatal cases of TSC. Three novel variants in TSC genes enlarge the variants spectrum of TSC.