ABC | Volume 112, Nº5, Maio 2019

Relato de Caso Kilit et al Síndrome de WPW em uma família com CFNS Arq Bras Cardiol. 2019; 112(5):594-596 1. Zafeiriou DI, Pavlidou EL, Vargìami E. Diverse clinical and genetic aspects of craniofrontonasal syndrome. Pediatr Neurol. 2011;44(2):83-7. 2. Twigg SR, Kan R, Babbs C, Bochukova EG, Robertson SP, Wall SA, et al. Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome. Proc Natl Acad Sci U S A. 2004;101(23):8652-7. 3. Guize L, Soria R, Chaouat JC, Chrétien JM, Houe D, Le Heuzey JY. [Prevalence and course of Wolf-Parkinson-White syndrome in a population of 138,048 subjects]. Ann Med Interne (Paris). 1985; 136(6):474-8. 4. MassumiRA.FamilialWolff-Parkinson-Whitesyndromewithcardiomyopathy. Am J Med. 1967;43(6):951-5. 5. Vidaillet HJ Jr, Pressley JC, Henke E, Harrell FE Jr, German LD. Familial occurrence of accessory atrioventricular pathways (preexcitation syndrome). N Engl J Med. 1987;317(2):65-9. 6. Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, et al. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N Engl J Med. 2001;344(24):1823-31. 7. Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, et al. Novel PRKAG2mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy. Circulation. 2001;104(25):3030-3. 8. Kullander K, Klein R. Mechanisms and functions of Eph and ephrin signalling. Nat Rev Mol Cell Biol. 2002;3(7):475-86. 9. Goyal M, Pradhan G, Wieland I, Kapoor S. Craniofrontonasal Syndrome: Atrial Septal Defect With a Novel EFNB1 Gene Mutation. Cleft Palate Craniofac J. 2015;52(2):234-6. 10. Chacon-Camacho OF, Arce-Gonzalez R, Villegas-Ruiz V, Pelcastre-Luna E, Uría-Gómez CE, Granillo-Alvarez M, et al. Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome. Meta Gene. 2013 Nov 28;2:25-31. Referências Este é um artigo de acesso aberto distribuído sob os termos da licença de atribuição pelo Creative Commons 596

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