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2014 | 4 | 2 | 20-23
Tytuł artykułu

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

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Interrupted aortic arch is a rare and very difficult to diagnose congenital heart defect, which is divided into three types according to the place of interruption. The most common is type B, where the interruption is between the left carotid artery and left subclavian artery. This case report shows the description of the anomaly during the first and second trimester scan and review of the literature regarding interrupted aortic arch.
Słowa kluczowe
Wydawca

Czasopismo
Rocznik
Tom
4
Numer
2
Strony
20-23
Opis fizyczny
Daty
wydano
2014-06-01
otrzymano
2014-05-14
zaakceptowano
2014-06-27
online
2015-12-30
Twórcy
  • Obstetrics and Perinatology Department, Collegium Medicum, Jagielonian University, Krakow, goroka@poczta.onet.pl
autor
  • Obstetrics and Perinatology Department, Collegium Medicum, Jagielonian University, Krakow
Bibliografia
  • 1. Celoria GC, Patton RB. Congenital absence of the aortic arch. Am Heart J 1959;58:407-413.[Crossref]
  • 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 Ginekologicznego w zakresie przesiewowej diagnostyki ultrasonograficznej w ciąży o przebiegu prawidłowym - 2012.
  • 5. Volpe P, Tuo G, De Robertis V, Campobasso G, Marasini M, Tempesta AA, Gentile M, Rembouskos G. Fetal interrupted aortic arch: 2D-4D echocardiography, associations and outcome. Ultrasound Obstet Gynecol 2010;35:302-309.[Crossref][WoS]
  • 6. Volpe P, Marasini M, Caruso G, Gentile M. Prenatal diagnosis of interruption of the aortic arch and its association with deletion of chromosome 22q11. Ultrasound Obstet Gynecol 2002;20:327-331.[Crossref]
  • 7. Vogel M, Vernon MM, MvElhinney DB, Brown DW, Colan SD, Tworetzky W. Fetal diagnosis of interrupted aortic arch. Am J Cardiol 2010;105:727-734.[Crossref]
  • 8. Turan S, Turan OM, Desai AA, Harman CR, Baschat AA. A prospective study of first trimester fetal cardiac examination using spatiotemporal image correlation, tomographic ultrasound and color Doppler imaging for the diagnosis of complex congenital heart disease in high-risk patients. Ultrasound Obstet Gynecol 2014;[Crossref][WoS]
  • 9. Słodki M, Rychik J, Moszura T, Janiak K, Respondek-Liberska M. Measurement of the great vessels in the mediastinum could help distinguish true from false-positive coarctation of the aorta in the third trimester. J Ultrasound Med 2009;28:1313-1317.
  • 10. Słodki M, Moszura T, Janiak K, Sysa A, Seligman NS, Weiner S, Respondek-Liberska M. The three-vessel view in the fetal miedistinum in the diagnosis of interrupted aortic arch. Ultrasound Med Biol 2011;37(11):1808-1813.[Crossref][WoS]
  • 11. Momma K. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol 2010;105:1617-1624.[Crossref]
  • 12. Volpe P, Marasini M, Caruso G, Marzullo A, Buonadonna AL, Arciprete P, Di Paolo S, Volpe G, Gentile M. 22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signs. Prenat Diagn 2003;23:752-757.
  • 13. Chaoui R, Kalache KD, Heling KS, Tennstedt C, Bommer C, Korner H. Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects. Ultrasound Obstet Gynecol 2002;20:546-552.[Crossref]
  • 14. Van Mierop LH, Kutsche LM. Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. Am J Cardiol 1986;58:133-137.[Crossref]
  • 15. Takahashi K, Kuwahara T, Nagatsu M. Interruption of the aortic arch at the isthmus with DiGeorge syndrome and 22q11.2 deletion. Cardiol Young 1999;9:516-518
  • 16. Lewin MB, Lindsay EA, Jurecic V, Goytia B, Towbin J, Baldini A. A genetic aetiology for interruption of the aortic arch type B. Am J Cardiol 1997;80: 493-497.[Crossref]
  • 17. Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zachai EH, Emanuel BS, Driscoll DA. Frequency of 22q11 deletions in patients with conotruncal defects. J Am Coll Cardiol 1998;32: 492-498.
  • 18. Oosterhof T, Azakie A, Freedom RM, Wiliams WG, McCrindle BW. Associated factors and trends in outcomes of interrupted aortic arch. Ann Thorac Surg 2004;78:1696-1702.[Crossref]
  • 19. Law KM, Tse KT. Prenatal sonographic diagnosis of familial Holt- Oram syndrome associated with type B interrupted aortic arch. Hong Kong Med J 2008;14:317-320.
  • 20. Ziolkowska L, Kawalec W, Turska-Kmiec A, Krajewska-Walasek M, Brzezinska-Rajszys G, Daszkowska J, Maruszewski B, Burczynski P. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery. Eur J Pediatr 2008;167:1135-1140. [Crossref][WoS]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_12847_06143
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