ABC | Volume 110, Nº1, January 2018

Review Article Oliveira et al Association of congenital heart diseases with ophthalmologic changes Arq Bras Cardiol. 2018; 110(1):84-90 35. Kondoh T, Okamoto N, Norimatsu N, Uetani M, Nishimura G, Moriuchi H. A Japanese case of oto-palato-digital syndrome type II: an apparent lack of phenotype-genotype correlation. J Hum Genet 2007;52(4):370-3. doi:10.1007/s10038-007-0108-7 36. Hanna NN, Eickholt K, Agamanolis D, Burnstine R, Edward DP. Atypical Peters plus syndrome with new associations. J AAPOS. 2010;14(2):181-3. doi: 10.1016/j.jaapos.2010.02.003. 37. Bajaj A, Dyke P, Zaleski C, Cava J, McPherson E. Tessier No. 7 cleft with PHACE syndrome: The case for pulmonary vascular steal. Am J Med Genet A. 2011;155A(9):2298-301. doi: 10.1002/ajmg.a.34166. 38. Scalais E, Verloes A, Sacré JP, Piérard GE, Rizzo WB. Sjogren-Larsson- like syndrome with bone dysplasia and normal fatty alcohol NAD(+) oxidoreductase activity. Pediatr Neurol. 1992;8(6):459-65. PMID:1476577 39. Vilela MA, Sbruzzi G, Pellanda LC. Prevalence of ophthalmological abnormalities in children and adolescents with CHD: systematic review and meta-analysis of observational studies. Cardiol Young. 2016;26(3):477-84. doi: 10.1017/S104795111500044X 40. Nisli K. Prevalence of congenital heart defects in patients with Down’s syndrome. J Pediatr (Rio J). 2009;85(5):377-8. doi:10.2223/JPED.1940. This is an open-access article distributed under the terms of the Creative Commons Attribution License 90