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The 1st and 2nd trimester scan of the fetal heart in the case of interrupted aortic arch - case report

References 1. Celoria GC, Patton RB. Congenital absence of the aortic arch. Am Heart J 1959;58:407-413. 2. Reardon MJ, Hallman GL, Cooley DA. Interrupted aortic arch: Brief review and summary of an eighteen-year experience. Tex Heart Inst J 1984;11:250-259. 3. Hornberger LK. Aortic arch anomalies. In: Textbook of Fetal Cardiology, Allan L, Hornberger L, Sharland G (eds). Greenwich Medical Media: London, 2000: 305-321. 4. Przewodnik po Rekomendacjach Sekcji Ultrasonografii Polskiego Towarzystwa

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Isolated Double Aortic Arch (Daa) – Prenatal Detection with Postnatal Follow-Up, Case Report and Literature Review

References 1. Hunter L., Callaghan N., Patel K., Prenatal echocardiographic diagnosis of double aortic arch, Ultrasound Obstet Gynecol. 2015; 45: 483-485 2. Gou Z., He Y., Zhang Y., et al., Prenatal diagnosis of fetal double aortic arch: report of a case, Int J Clin Exp Pathol 2015; 8 (10): 13565-13567 3. Wójtowicz A., Respondek- Liberska M., et al., The significance of a prenatal diagnosis of right aortic arch, Prenatal diagnosis 2017; 37 (4): 365-374 4. Slodki M, Moszura T, Janiak K, Sysa A

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Comparison of the clinical status and the effects of treatment of newborns with interrupted aortic arch diagnosed prenatally and postnatally in the "Polish Mother's Memorial" Institute in Lodz in the years 2003-2012

References 1. Skalski J, Religa Z. Kardiochirurgia dziecięca. Wydawnictwo Naukowe Śląsk, Katowice 2003. 2. Malec E, Januszewska K, Radziwiłłowa D, Pawłowska M. Dziecko z wadą serca. Poradnik dla rodziców. Fundacja im. Diny Radziwiłłowej, Warszawa 2007. 3. Dillman J, Yarram S, D’Amico A, i wsp. Interrupted Aortic Arch. Spectrum of MRI Findings. American Journal of Roentgenology 2008;6(190):1467-1474. 4. Szczeklik A, Tender M. Kariologia. Podręcznik oparty na zasadach EBM. Tom I. Wyd. Medycyna

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Great Vessels Anomalies – Prenatal Echocardiography and Neonatal Angio-CT – A Pictorial Essay

. 10. Zhang D, Zhang Y, Ren W, Sun F, Guo Y, Sun W, Wang Y, Huang L, Cai A. Prenatal Diagnosis of Fetal Interrupted Aortic Arch Type A by Two-Dimensional Echocardiography and Four-Dimensional Echocardiography with B-Flow Imaging and Spatiotemporal Image Correlation. Echocardiography. 2016 Jan;33(1):90-8. doi: 10.1111/echo.12996. Epub 2015 Jun 22. 11. Manganaro L. State of art of MRI of fetal heart in 2015. Prenat Cardio. 2015 Sep;5(3):9-12 Doi 10.12847/09152. 12. Slodki M, Moszura T, Janiak K, Sysa A, Seligman NS, Weiner S, Respondek

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Cases Report. Missed Diagnoses in Prenatal Evaluation by Ultrasound: A Retrospective Analysis of four Cases from a Tertiary Center for Fetal Malformations


Four cases of missed prenatal diagnosis by an experienced ultrasonographer and a fetal cardiologist from a tertiary teaching hospital are presented: 3-mm peri-membrane ventricular septal defect; hypoplastic aortic arch requiring prostin infusion after delivery; esophageal atresia with tracheal fistula; and right-sided diaphragmatic hernia. Freezed frames and cine loops of the prenatal ultrasound scans indicated that the missed anomalies were not visible in midgestation, suggesting that in the future, repeat ultrasound scans should be performed before delivery to reduce the occurrence of such diagnostic errors.

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Prenatal Diagnosis of Holt-Oram Syndrome

the Holt-Oram syndrome. Prenat Diagn. 1988, 3 (8): 175-181 3. Law KM, Tse KT.: Prenatal sonographic diagnosis of familial Holt-Oram syndrome associated with type B interrupted aortic arch. Hong Kong Med J. 2008, 4 (14): 317-320 4. GeneReviews 5. Sunagawa S, Kikuchi A, Sano Y, Kita M, Ono K, Horikoshi T, Takagi K, Kawame H.: Prenatal diagnosis of Holt-Oram syndrome: role of 3-D ultrasonography. Congenit Anom (Kyoto) 2009, 1 (49): 38-41 6

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Prenatal Detection and Postnatal Verification of Unusual Intracardiac Total Anomolous Pulmonary Venous Connection (Tapvc) in Complex Heart Defect with Dextrocardia - Case Report

aortic arch. Ultrasound Med Biol 2011: 37 (11): 1808-1813 11. Słodki M, Janiak K, Moszura T, Respondek-Liberska M. View of fetal mediastinum in the diagnosis of coarctation and interrupted aortic arch. Kardiologia Prenatalna ECHO PŁODU-2010, 15-16. ADI, Łódź 2010. 12. Respondek-Liberska M, Szymkiewicz-Dangel J, Tobota Z, Słodki M. Założenia i wstępne wnioski Ogólnopolskiego Rejestru Patologii Kardiologicznych u płodu. Polski Przegląd Kardiologiczny 2008, 10; 129-135. 13. Paladini D, Pistorio A, Wu LH, Meccariello G, Lei T

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Selected data from the Polish National Prenatal Cardiac Pathology Registry from the year 2016

.1002/uog.17469. [Epub ahead of print] 25. 26. Wójtowicz A, Respondek-Liberska M, Słodki M, Kordjalik P, Płużańska J, Knafel A, Huras H. The significance of a prenatal diagnosis of right aortic arch. Prenat Diagn. 2017; 37: 365-374 27. Materna-Kiryluk A.: Polish Registry of Congenital Malformations as a source of epidemiology, etiology and plans for medical care. Medical University K. Marcinkowskiego, Poznań 2014 28. Górska-Kot A1, Błaz W, Pszeniczna E, Rusin J, Materna-Kiryluk A

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Assessment of the accuracy in prenatal diagnosis of congenital malformations. Analysis of 101 questionnaires filled in by parents of neonates hospitalized in the Department of Congenital Malformations Polish Mother's Memorial Research Institute

from false-positive coarctation of the aorta in the third trimester. J Ultrasound Med. 2009, 28,1313-7 19. Respondek-Liberska M, Sysa A, Gadzinowski J: Financial comparison of neonatal transportation: in utero, by ambulance and by air transportation. Ginekol. Pol. 2004, 75, 326- 331 20. Chaoi R, Rake A, Heling KS. Aortic arch with four vessels: Aberrant right subclavian artery.Ultrasound Obstet Ginecol. 2008,31,115-117. 21. Allan LD, Crawford DC, Chita SK. Prenatal screening for congenital heart disease. British Medical

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An Outline of Cardiogenesis

H, Morishima M, Huynh T, Pramparo T, Jurecic V, Ogunrinu G, Sutherland HF, Scambler PJ, et al. (2001). Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice. Nature 410:97-101. 8. Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, et al. (2001). TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell 104: 619-629. 9. Mori AD, Bruneau BG (2004). TBX5 mutations and congenital heart disease: Holt-Oram syndrome

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