⌘+K

Pulse Explore Communities Researchers Journals

Home Communities Explore

November 24, 2025BMC Pregnancy and ChildbirthOpen Access

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

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

View Full Paper

Ask AI

Bookmark

Share

Abstract

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.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Liu et al. (2025) studied this question.

synapsesocial.com/papers/69403db02d562116f290de9c https://doi.org/10.1186/s12884-025-08365-7

View Full Paper

Ask AI

Bookmark

Share

Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Whole exome sequencing in fetal cardiac rhabdomyoma detected by ultrasonography: an analysis of 12 cases2025
2Whole Exome Sequencing in Fetal Cardiac Rhabdomyoma Detected by Ultrasonography: An Analysis of 12 Cases2025
3Prenatal diagnosis of cardiac rhabdomyoma: implications for predicting tuberous sclerosis complex and guiding perinatal managementCohort Study · 2026
4Case Report: Fetal cardiac rhabdomyoma caused by TSC1 mutation2025 · 1 citations
5Prenatal diagnosis and clinical management of cardiac rhabdomyoma: a single-center study2024 · 15 citations

More related papers

Prenatal diagnosis and outcomes of fetal cardiac tumors: a 10-year single-center study of 81 cases2026
Fetal and neonatal cardiac tumor diagnosed as Tuberous Sclerosis associated rhabdomyomas resulting from novel pathogenic missense variant detected in TSC2 gene: A case report2024
Prenatal diagnosis of fetal cardiac rhabdomyoma associated with tuberous sclerosis: A case report2018

More from BMC Pregnancy and Childbirth

Association of maternal homocysteine and coagulation–fibrinolysis biomarkers with small-for-gestational-age birth in pregnancies complicated by gestational diabetes mellitus and preeclampsiaThu,
IFI44L promoter hypomethylation is associated with a clinically defined immune-inflammatory phenotype in recurrent pregnancy lossWed,