Válvula aórtica bicúspide en lactantes, niños, y adolescentes

1. Hoffman JI, Kaplan S. The incidence of congenital heart disease. J Am Coll Cardiol . 2002;39(12):1890–1900

2. Fernandes SM, Sanders SP, Khairy P, et al. Morphology of bicuspid aortic valve in children and adolescents. J Am Coll Cardiol . 2004;44(8):1648–1651 3. Michelena HI, Desjardins VA, Avierinos JF, et al. Natural history of asymptomatic patients with normally functioning or minimally dysfunctional bicuspid aortic valve in the community. Circulation . 2008;117(21):2776–2784

4. Verma S, Siu SC. Aortic dilatation in patients with bicuspid aortic valve. N Engl J Med. 2014;370(20):1920–1929

5. Niaz T, Poterucha JT, Johnson JN, et al. Incidence, morphology, and progression of bicuspid aortic valve in pediatric and young adult subjects with coexisting congenital heart defects. Congenit Heart Dis. 2017;12(3):261–269

6. Fernandes SM, Khairy P, Sanders SP, Colan SD. Bicuspid aortic valve morphology and interventions in the young. J Am Coll Cardiol . 2007;49(22):2211–2214

7. Beaton AZ, Nguyen T, Lai WW, et al. Relation of coarctation of the aorta to the occurrence of ascending aortic dilation in children and young adults with bicuspid aortic valves. Am J Cardiol . 2009;103(2):266–270

8.McElhinney DB, Petrossian E, Tworetzky W, Silverman NH, Hanley FL. Issues and outcomes in the management of supravalvar aortic stenosis. Ann Thorac Surg. 2000; 69 (2):562–567

9.Sharma BK, Fujiwara H, Hallman GL, Ott DA, Reul GJ, Cooley DA. Supravalvar aortic stenosis: a 29-year review of surgical experience. Ann Thorac Surg. 1991;51(6):1031–1039

10.van Son JAM, Danielson GK, Puga FJ, et al. Supravalvular aortic stenosis: long-term results of surgical treatment. J Thorac Cardiovasc Surg. 1994;107(1):103–114, discussion 114–115

11. Silberbach M, Roos-Hesselink JW, Andersen NH, et al; American Heart Association Council on Cardiovascular Disease in the Young; Council on Genomic and Precision Medicine; and Council on Peripheral Vascular Disease. Cardiovascular health in Turner syndrome: a scientific statement from the American Heart Association. Circ Genom Precis Med. 2018;11(10):e000048

12.Collins RT II, Kaplan P, Somes GW, Rome JJ. Cardiovascular abnormalities, interventions, and long-term outcomes in infantile Williams syndrome. J Pediatr . 2010;156(2):253–8.e1

13.Collins RT II. Cardiovascular disease in Williams syndrome. Curr Opin Pediatr . 2018;30(5):609–615

14.Nistri S, Porciani MC, Attanasio M, Abbate R, Gensini GF, Pepe G. Association of Marfan syndrome and bicuspid aortic valve: frequency and outcome. Int J Cardiol . 2012;155(2):324–325

15.Patel ND, Alejo D, Crawford T, et al. Aortic root replacement for children with Loeys-Dietz syndrome. Ann Thorac Surg. 2017;103(5):1513–1518

16.Rauser-Foltz KK, Starr LJ, Yetman AT. Utilization of echocardiography in Ehlers-Danlos syndrome. Congenit Heart Dis. 2019;14(5):864–867

17. Niaz T, Poterucha JT, Olson TM, et al. Characteristic morphologies of the bicuspid aortic valve in patients with genetic syndromes. J Am Soc Echocardiogr. 2018;31(2):194–200

18. Huntington K, Hunter AG, Chan KL. A prospective study to assess the frequency of familial clustering of congenital bicuspid aortic valve. J Am Coll Cardiol . 1997;30(7):1809–1812 19. Cripe L, Andelfinger G, Martin LJ, Shooner K, Benson DW. Bicuspid aortic valve is heritable. J Am Coll Cardiol . 2004;44(1):138–143

20. Kerstjens-Frederikse WS, Du Marchie Sarvaas GJ, Ruiter JS, et al. Left ventricular outflow tract obstruction: should cardiac screening be offered to first-degree relatives? Heart. 2011;97(15):1228–1232

21. Freeze SL, Landis BJ, Ware SM, Helm BM. Bicuspid aortic valve: a review with recommendations for genetic counseling. J Genet Couns. 2016;25(6):1171–1178

22. Prakash SK, Bossé Y, Muehlschlegel JD, et al; BAVCon Investigators. A roadmap to investigate the genetic basis of bicuspid aortic valve and its complications: insights from the International BAVCon (Bicuspid Aortic Valve Consortium). J Am Coll Cardiol . 2014;64(8):832–839

23. Kelle AM, Qureshi MY, Olson TM, Eidem BW, O’Leary PW. Familial incidence of cardiovascular malformations in hypoplastic left heart syndrome. Am J Cardiol . 2015;116(11):1762–1766

24. Mills P, Leech G, Davies M, Leathan A. The natural history of a non-stenotic bicuspid aortic valve. Br Heart J. 1978;40(9):951–957

25. Eckhauser A, South ST, Meyers L, Bleyl SB, Botto LD. Turner syndrome in girls presenting with coarctation of the aorta. J Pediatr . 2015;167(5):1062–1066 Open URL Google Scholar

26. Wong SC, Burgess T, Cheung M, Zacharin M. The prevalence of Turner syndrome in girls presenting with coarctation of the aorta. J Pediatr . 2014;164(2):259–263

27. Siu SC, Silversides CK. Bicuspid aortic valve disease. J Am Coll Cardiol . 2010;55(25):2789–2800

28. Chan KL, Stinson WA, Veinot JP. Reliability of transthoracic echocardiography in the assessment of aortic valve morphology: pathological correlation in 178 patients. Can J Cardiol . 1999;15(1):48–52

29. Tanaka R, Yoshioka K, Niinuma H, Ohsawa S, Okabayashi H, Ehara S. Diagnostic value of cardiac CT in the evaluation of bicuspid aortic stenosis: comparison with echocardiography and operative findings. AJR Am J Roentgenol. 2010;195(4):895–899