References
- Hoffman JIE, Kaplan S. The incidence of congenital heart disease. J Am Coll Cardiol. 2002;39(12):1890–1900.
- Abuhamad AZ, Chaoui R. A practical guide to fetal echocardiography: normal and abnormal hearts. 3rd ed. Philadelphia: Wolters Kluwer; 2016.
- Donofrio MT, Moon-Grady AJ, Hornberger LK, et al. Diagnosis and treatment of fetal cardiac disease. Circulation. 2014;129(21):2183–2242.
- Gilboa SM, Salemi JL, Nembhard WN, et al. Mortality resulting from congenital heart disease among children and adults in the United States, 1999 to 2006. Circulation. 2010;122(22):2254–2263.
- Carvalho JS, Mavrides E, Shinebourne EA, et al. Improving the effectiveness of routine prenatal screening for major congenital heart defects. Heart. 2002;88(4):387–391.
- Ionescu CA, Vladareanu S, Tudorache S, et al. The wide spectrum of ultrasound diagnosis of holoprosencephaly. Med Ultrason. 2019;21(2):163–169.
- Herghelegiu D, Ionescu CA, Pacu I, et al. Antenatal diagnosis and prognostic factors of aneurysmal malformation of the vein of Galen: A case report and literature review. Medicine (Baltimore). 2017;96(30):e7483.
- Gembruch U, Knöpfle G, Chatterjee M, et al. First-trimester diagnosis of fetal congenital heart disease by transvaginal two-dimensional and Doppler echocardiography. Obstet Gynecol. 1990;75(3 Pt 2):496–498.
- Becker R, Wegner R-D. Detailed screening for fetal anomalies and cardiac defects at the 11–13-week scan. Ultrasound Obstet Gynecol. 2006;27(6):613–618.
- Wiechec M, Knafel A, Nocun A. Prenatal detection of congenital heart defects at the 11- to 13-week scan using a simple color doppler protocol including the 4-chamber and 3-vessel and trachea views. J Ultrasound Med. 2015;34(4):585–594.
- Veduta A, Vayna AM, Duta S, et al. The first trimester combined test for aneuploidies–a single center experience. J Matern Neonatal Med. 2018;31(16):2091–2096.
- Hutchinson D, McBrien A, Howley L, et al. First-trimester fetal echocardiography: identification of cardiac structures for screening from 6 to 13 weeks’ gestational age. J Am Soc Echocardiogr. 2017;30(8):763–772.
- Syngelaki A, Chelemen T, Dagklis T, et al. Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks. Prenat Diagn. 2011;31(1):90–102.
- Herghelegiu CG, Dragan I, Suciu N, et al. A simplified protocol for congenital heart disease. Proceedings of the 5th Romanian Congress of Ultrasound in Obstetrics and Gynecology. 2017. p. 298–302.
- Jicinska H, Vlasin P, Jicinsky M, et al. Does first-trimester screening modify the natural history of congenital heart disease? Circulation. 2017;135(11):1045–1055.
- Comstock CH. Normal fetal heart axis and position. Obstet Gynecol. 1987;70(2):255–259.
- Iliescu D, Tudorache S, Comanescu A, et al. Improved detection rate of structural abnormalities in the first trimester using an extended examination protocol. Ultrasound Obstet Gynecol. 2013;42(3):300–309.
- Persico N, Moratalla J, Lombardi CM, et al. Fetal echocardiography at 11–13 weeks by transabdominal high-frequency ultrasound. Ultrasound Obstet Gynecol. 2011;37(3):296–301.
- Duta S, Veduta A, Vayna AM, et al. The outcome of structural heart defects diagnosed in the first trimester of pregnancy. J Matern Neonatal Med. 2019;7:1–6.
- Vayna AM, Veduta A, Duta S, et al. Diagnosis of fetal structural anomalies at 11 to 14 weeks. J Ultrasound Med. 2018;37(8):2063–2073.
- Perde F, Herghelegiu CG, Iosifescu AG, et al. Pulmonary artery aneurysm in a marfanoid adult patient with unoperated functional single ventricle and levo-transposition of the great arteries. Rom J Leg Med. 2018;26:363–368.