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Goldenhar syndrome with right circumflex aortic arch, severe coarctation and vascular ring in a twin pregnancy


Department of Pediatric Cardiology, Children's Medical Center (Pediatrics Center of Excellence), Tehran University of Medical Sciences, Tehran, Iran

Correspondence Address:
Elaheh Malakan Rad
Department of Pediatric Cardiology, Children's Medical Center (Pediatrics Center of Excellence), Tehran University of Medical Sciences, Tehran
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0974-2069.140857

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Year : 2014  |  Volume : 7  |  Issue : 3  |  Page : 217-220

 

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Goldenhar syndrome (GS) or oculo-auriculo-vertebral dysplasia (OAVD), involves a wide variety of organ systems. Cardiovascular anomalies are among the frequent malformations. The purpose of this report is to introduce a male case of a dizygotic twin pregnancy with GS and right circumflex aortic arch (RCAA), severe coarctation, hypoplastic aortic arch, aberrant right subclavian artery, vascular ring, bilateral renal artery stenosis, and mild Dandy-Walker syndrome. The embryology of RCAA and coarctation is revisited.






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Department of Pediatric Cardiology, Children's Medical Center (Pediatrics Center of Excellence), Tehran University of Medical Sciences, Tehran, Iran

Correspondence Address:
Elaheh Malakan Rad
Department of Pediatric Cardiology, Children's Medical Center (Pediatrics Center of Excellence), Tehran University of Medical Sciences, Tehran
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0974-2069.140857

Rights and Permissions

Goldenhar syndrome (GS) or oculo-auriculo-vertebral dysplasia (OAVD), involves a wide variety of organ systems. Cardiovascular anomalies are among the frequent malformations. The purpose of this report is to introduce a male case of a dizygotic twin pregnancy with GS and right circumflex aortic arch (RCAA), severe coarctation, hypoplastic aortic arch, aberrant right subclavian artery, vascular ring, bilateral renal artery stenosis, and mild Dandy-Walker syndrome. The embryology of RCAA and coarctation is revisited.






[FULL TEXT] [PDF]*


        
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