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A Pipeline to Characterize Structural Heart Defects in the Fetal Mouse
Published on: December 16, 2022
Natural history of prenatal isolated muscular ventricular septal defects
Onur Erol1, Osman Sevket2, Seda Keskin2
1Department of Obstetrics and Gynecology, Antalya Training and Research Hospital, Antalya, Turkey.
Insights
Muscular ventricular septal defects (m-VSDs) show a high spontaneous closure rate within the first year of life. Small m-VSDs, particularly those ≤3 mm, frequently resolve during gestation or early infancy.
Area of Science:
- Pediatric Cardiology
- Fetal Medicine
- Congenital Heart Disease
Background:
- Muscular ventricular septal defects (m-VSDs) are a subset of congenital heart defects.
- Understanding their natural history is crucial for clinical management and parental counseling.
Purpose of the Study:
- To evaluate the natural history of isolated muscular ventricular septal defects (m-VSDs).
- To assess spontaneous closure rates from gestation up to one year postnatally.
- To investigate the association between m-VSDs and chromosomal anomalies.
Main Methods:
- A cohort of 76 fetuses with isolated m-VSDs was studied.
- Evaluated variables included defect site, size, chromosomal anomalies, pregnancy outcome, and postnatal closure.
- Follow-up extended to one year postnatally for closure assessment.
Main Results:
- Of 44 fetuses reaching one year, 75% of m-VSDs closed spontaneously.
- Small defects (≤3 mm) demonstrated a high closure rate (83.8%) during gestation or the first year.
- Apical defects showed a trend towards more frequent spontaneous closure, though not statistically significant compared to mid-muscular defects.
Conclusions:
- Isolated muscular ventricular septal defects exhibit a high rate of spontaneous closure.
- Small m-VSDs are particularly likely to close spontaneously, often before or within the first year after birth.
Objective:
To evaluate the natural history of isolated muscular ventricular septal (m-VSD) defects during gestation and up to 1 year postnatally, as well as the association with chromosomal anomalies.
Material And Methods:
Between August 2007 and July 2012, 76 fetuses with isolated m-VSDs represented the study population. The following variables were evaluated: site and size of the m-VSDs, presence of chromosomal anomalies, pregnancy outcome, and spontaneous closure rate from diagnosis up to 1 year postnatally.
Results:
Of the 76 cases with m-VSD, 1 fetus died after birth and 31 cases were lost to follow-up after birth. Thus, a total of 44 fetuses reached their first year of postnatal life, and these cases were available for analysis. Three (6.8%) of 44 defects closed spontaneously in utero, 33 (75%) closed within 1 year, and 8 (18.2%) remained patent. Overall, spontaneous closure occurred more frequently in the apical defects, but no significant difference was found for spontaneous closure between the mid-muscular and apical defects (p>0.05). Also, 83.8% (36 of 44) of defects ≤3 mm closed during gestation or the first year of life.
Conclusion:
We infer that m-VSDs have a high spontaneous closure rate during the first year of life. Also, small m-VSDs frequently close spontaneously.
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