مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

PRENATAL DIAGNOSIS OF DOUBLE ARCUS AORTA ANOMALIES: CASE REPORT

Pages

  45-46

Abstract

 Introduction: Double aortic arch is a rare CARDIAC anomaly that constitutes 1% to 3% of all CONGENITAL ANOMALIES. Prenatal diagnoses of such conditions are rare.Case Presentation: We present a case of double aortic arch with compression of the trachea that was diagnosed during the 20th week of gestation. The baby was delivered during the 29th week of gestation via cesarean and the diagnosis was confirmed with computerized tomography (CT) angiography. Later, a surgical repair was undertaken; however, the patient succumbed to pulmonary complications 3 months after delivery.Conclusions: Aortic arch anomalies are a rare and diverse group of congenital heart anomalies. PRENATAL DIAGNOSIS is possible and beneficial in cases with tracheal compression as it allows for early intervention after birth.

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  • Cite

    APA: Copy

    YUCE, TUNCAY, KALAFAT, ERKAN, & KOC, ACAR. (2016). PRENATAL DIAGNOSIS OF DOUBLE ARCUS AORTA ANOMALIES: CASE REPORT. INTERNATIONAL JOURNAL OF WOMEN’S HEALTH AND REPRODUCTION SCIENCES, 4(1), 45-46. SID. https://sid.ir/paper/334451/en

    Vancouver: Copy

    YUCE TUNCAY, KALAFAT ERKAN, KOC ACAR. PRENATAL DIAGNOSIS OF DOUBLE ARCUS AORTA ANOMALIES: CASE REPORT. INTERNATIONAL JOURNAL OF WOMEN’S HEALTH AND REPRODUCTION SCIENCES[Internet]. 2016;4(1):45-46. Available from: https://sid.ir/paper/334451/en

    IEEE: Copy

    TUNCAY YUCE, ERKAN KALAFAT, and ACAR KOC, “PRENATAL DIAGNOSIS OF DOUBLE ARCUS AORTA ANOMALIES: CASE REPORT,” INTERNATIONAL JOURNAL OF WOMEN’S HEALTH AND REPRODUCTION SCIENCES, vol. 4, no. 1, pp. 45–46, 2016, [Online]. Available: https://sid.ir/paper/334451/en

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