Percutaneous closure of isolated ostium secundum-type atrial septal defect in a patient with Mayer-Rokitansky-Küster-Hauser syndrome

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• 作者：Murat Akcay^a ; ^{drmuratakcay@hotmail.com} ; Okan Gulel^b ; Korhan Soylu^b ; Murat Meric^b ; Muzaffer Elmali^c
• 关键词：Atrial septal defect ; Mayer-Rokitansky-Kü ; ster-Hauser syndrome ; Percutaneous closure
• 刊名：Revista Portuguesa de Cardiologia (English Edition)
• 出版年：2016
• 出版时间：December 2016
• 年：2016
• 卷：35
• 期：12
• 页码：701.e1-701.e3
• 全文大小：442 K
• 卷排序：35

文摘

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital anomaly characterized by complete or partial aplasia of the uterus and the upper part of the vagina. It is reported to be associated with cardiovascular disorders including atrial septal defect, anomalous pulmonary venous return, aortopulmonary window, pulmonary valve stenosis, mitral valve prolapse, tetralogy of Fallot, truncus arteriosus, and patent ductus arteriosus. Herein, for the first time in the medical literature, we present percutaneous closure of an isolated ostium secundum atrial septal defect in this syndrome.