A Case With Dextrocardia and Multiple Cardiac Anomalies in a Family With Congenital Heart Malformations

被引：0

作者：

Ceylaner, Serdar ^{[1
]}

Guven, Melih Atahan ^{[2
]}

Ceylaner, Gulay ^{[1
]}

Ciragil, Gokhan ^{[3
]}

Tug, Mengu ^{[4
]}

Ertas, I. Egemen ^{[5
]}

机构：

[1] Zekai Tahir Burak Womens Hlth Educ & Res Hosp, Dept Genet, Ankara, Turkey

[2] Kahramanmaras Sutcuimam Univ, Fac Med, Dept Obstet & Gynecol, Kahramanmaras, Turkey

[3] Kahramanmaras State Hosp, Dept Obstet & Gynecol, Kahramanmaras, Turkey

[4] Zekai Tahir Burak Womens Hlth Educ & Res Hosp, Dept Pathol, Ankara, Turkey

[5] Zekai Tahir Burak Womens Hlth Educ & Res Hosp, Dept Obstet & Gynecol, Ankara, Turkey

来源：

JOURNAL OF THE TURKISH-GERMAN GYNECOLOGICAL ASSOCIATION | 2005年 / 6卷 / 02期

关键词：

dextrocardia; heart defects; congenital; pregnancy; genetic counselling; prenatal diagnosis;

D O I：

暂无

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

In this case; an interesting example of family with recurrent congenital heart defects due to situs ambiguous has been presented. The parents were relatives and had a history of termination because of complex congenital cardiac malformations in the first pregnancy. Dextrocardia and complex malformations of the heart and great vessels were detected in the second pregnacy by fetal echocardiography at 23rd weeks of gestation. Postmortem evaluation confirmed prenatal findings on fetal echocardiography and also revealed medially placed liver, dextrocardia and a spleen on normal location. We suggest that all cases with complex congenital malformations of heart and/or great vessels must be assessed for the heterotaxy disorders because of the findings in this family.

引用

页码：158 / 160

页数：3

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