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Published on: February 11, 2022
Congenital medium sternal cleft with partial ectopia cordis repair
Paulo Rego Sousa1, Sónia Antunes, Alexandra Couto
1Hospital Central do Funchal, Rua da Rochinha, Rochinha Village, No. 109-casa B, Funchal, 9060-280, Portugal.
This case report details a rare congenital sternal cleft with ectopia cordis in a newborn. Early surgical repair shortly after birth led to a successful outcome, highlighting the benefits of prompt intervention for sternal malformations.
Area of Science:
- Pediatric Surgery
- Congenital Malformations
- Cardiothoracic Surgery
Background:
- Congenital sternal malformations are rare anomalies.
- Often diagnosed asymptomatically at birth.
- Includes conditions like sternal clefts and ectopia cordis.
Purpose of the Study:
- To report a clinical case of congenital sternal cleft with partial ectopia cordis.
- To emphasize the importance of early surgical intervention.
- To highlight successful surgical outcomes in neonates.
Main Methods:
- Case report of a full-term female neonate.
- Diagnosis of congenital sternal cleft and partial ectopia cordis.
- Surgical repair performed at 6 days of age.
Main Results:
- Successful surgical repair of the congenital sternal defect.
- Achieved favorable outcomes due to early intervention.
- Demonstrated the feasibility and benefits of neonatal surgery.
Conclusions:
- Early surgical repair in neonates facilitates easier procedures.
- Prompt intervention leads to better outcomes for congenital sternal malformations.
- This case underscores the effectiveness of timely surgical correction.
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