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Double orifice mitral valve: A rare cause of isolated severe congenital mitral regurgitation


1 Department of Pediatric Cardiac Surgery, Asian Institute of Medical Sciences, Faridabad, Haryana, India
2 Department of Pediatric Cardiology, Asian Institute of Medical Sciences, Faridabad, Haryana, India
3 Department of Pediatric Cardiac Intensive Care, Asian Institute of Medical Sciences, Faridabad, Haryana, India

Correspondence Address:
Dr. Himanshu Pratap
Department of Pediatric Cardiac Surgery, Asian Institute of Medical Sciences, Faridabad, Haryana
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_133_19

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Year : 2020  |  Volume : 13  |  Issue : 2  |  Page : 174-176

 

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Double orifice mitral valve (DOMV) is a rare congenital anomaly of the mitral valve apparatus consisting of an accessory bridge of fibrous tissue, which partially or completely divides the mitral valve into two orifices. It usually occurs as an associated lesion. Encountering a DOMV as an isolated finding meriting intervention is indeed rare. We, here, report a case of “complete bridging type DOMV” occurring as an isolated entity and presenting as severe congenital MR requiring surgery.






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1 Department of Pediatric Cardiac Surgery, Asian Institute of Medical Sciences, Faridabad, Haryana, India
2 Department of Pediatric Cardiology, Asian Institute of Medical Sciences, Faridabad, Haryana, India
3 Department of Pediatric Cardiac Intensive Care, Asian Institute of Medical Sciences, Faridabad, Haryana, India

Correspondence Address:
Dr. Himanshu Pratap
Department of Pediatric Cardiac Surgery, Asian Institute of Medical Sciences, Faridabad, Haryana
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_133_19

Rights and Permissions

Double orifice mitral valve (DOMV) is a rare congenital anomaly of the mitral valve apparatus consisting of an accessory bridge of fibrous tissue, which partially or completely divides the mitral valve into two orifices. It usually occurs as an associated lesion. Encountering a DOMV as an isolated finding meriting intervention is indeed rare. We, here, report a case of “complete bridging type DOMV” occurring as an isolated entity and presenting as severe congenital MR requiring surgery.






[FULL TEXT] [PDF]*


        
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