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This case report discusses a 1.5-year-old girl with absent left common carotid artery and cervical origin of the right subclavian artery, who developed symptomatic hemorrhage after surgery for Tetralogy of Fallot. The anomalies were discovered during embolization of aorto-pulmonary collaterals and are considered rare, with potential implications for embryological development and clinical significance. The child

Author

Vishal Nimbal

Language

EN