Literature DB >> 376232

Right aortic arch with isolation of left innominate artery.

M K Park.   

Abstract

A new entity of right aortic arch with isolation of the left innominate artery is described in a three-day-old boy with complete endocardial cushion defect. Embryologically, this type of anomaly will result if the interruption of the embryonic left aortic arch occurs at two sites, one between the left ductus arteriosus and the descending aorta and the other between the ascending aorta and the left common carotid artery. Absence of pulse in the left arm and on the left side of the neck strongly suggests this anomaly. The aortogram and pulmonary arteriogram may confirm the diagnosis of this anomaly during life.

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Year:  1979        PMID: 376232     DOI: 10.1378/chest.76.1.106

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  3 in total

1.  Left common carotid artery arising from the pulmonary artery in a patient with DiGeorge syndrome.

Authors:  S F Huang; M H Wu
Journal:  Heart       Date:  1996-07       Impact factor: 5.994

Review 2.  Aortic arch anomalies, embryology and their relevance in neuro-interventional surgery and stroke: A review.

Authors:  Shilpa S Mantri; Bharath Raju; Fareed Jumah; Michael S Rallo; Anmol Nagaraj; Priyank Khandelwal; Sudipta Roychowdhury; David Kung; Anil Nanda; Gaurav Gupta
Journal:  Interv Neuroradiol       Date:  2021-09-13       Impact factor: 1.764

3.  Right aortic arch with isolation of the left innominate artery in a case of double chamber right ventricle and ventricular septal defect.

Authors:  Chirantan Mangukia; Sonali Sethi; Saket Agarwal; Smita Mishra; Deepak Kumar Satsangi
Journal:  Ann Pediatr Cardiol       Date:  2014-05
  3 in total

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