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Trisomy 13 (Patau syndrome) and congenital heart defects
2013; Wiley; Volume: 164; Issue: 1 Linguagem: Inglês
10.1002/ajmg.a.36193
ISSN1552-4833
AutoresJanaina Borges Polli, Daniela de Paoli Groff, Patrícia Petry, Vinícius Freitas de Mattos, Rosana C. M. Rosa, Paulo Ricardo Gazzola Zen, Carla Graziadio, Giorgio Adriano Paskulin, Rafael Fabiano Machado Rosa,
Tópico(s)Congenital Heart Disease Studies
ResumoAmerican Journal of Medical Genetics Part AVolume 164, Issue 1 p. 272-275 Research Letter Trisomy 13 (Patau syndrome) and congenital heart defects Janaina B. Polli, Janaina B. Polli Pediatrics Service, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, BrazilSearch for more papers by this authorDaniela de P. Groff, Daniela de P. Groff Pediatrics Service, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, BrazilSearch for more papers by this authorPatrícia Petry, Patrícia Petry Pediatrics Service, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, BrazilSearch for more papers by this authorVinícius F. Mattos, Vinícius F. Mattos Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, BrazilSearch for more papers by this authorRosana C. M. Rosa, Rosana C. M. Rosa Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorPaulo R. G. Zen, Paulo R. G. Zen Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorCarla Graziadio, Carla Graziadio Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorGiorgio A. Paskulin, Giorgio A. Paskulin Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorRafael F. M. Rosa, Corresponding Author Rafael F. M. Rosa Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, Brazil Clinical Genetics, HMIPV, Porto Alegre, RS, Brazil Correspondence to: Rafael Fabiano Machado Rosa, M.D., PhD., Genética Clínica, UFCSPA/CHSCPA, Rua Sarmento Leite, 245/403, CEP: 90050-170, Porto Alegre, RS, Brazil. E-mail: [email protected]Search for more papers by this author Janaina B. Polli, Janaina B. Polli Pediatrics Service, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, BrazilSearch for more papers by this authorDaniela de P. Groff, Daniela de P. Groff Pediatrics Service, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, BrazilSearch for more papers by this authorPatrícia Petry, Patrícia Petry Pediatrics Service, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, BrazilSearch for more papers by this authorVinícius F. Mattos, Vinícius F. Mattos Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, BrazilSearch for more papers by this authorRosana C. M. Rosa, Rosana C. M. Rosa Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorPaulo R. G. Zen, Paulo R. G. Zen Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorCarla Graziadio, Carla Graziadio Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorGiorgio A. Paskulin, Giorgio A. Paskulin Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, BrazilSearch for more papers by this authorRafael F. M. Rosa, Corresponding Author Rafael F. M. Rosa Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, Brazil Clinical Genetics, HMIPV, Porto Alegre, RS, Brazil Correspondence to: Rafael Fabiano Machado Rosa, M.D., PhD., Genética Clínica, UFCSPA/CHSCPA, Rua Sarmento Leite, 245/403, CEP: 90050-170, Porto Alegre, RS, Brazil. E-mail: [email protected]Search for more papers by this author First published: 08 November 2013 https://doi.org/10.1002/ajmg.a.36193Citations: 12Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL REFERENCES Baty BJ, Blackburn BL, Carey JC. 1994. Natural history of trisomy 18 and trisomy 13: I. Growth, physical assessment, medical histories, survival, and recurrence risk. Am J Med Genet 49: 175– 188. Botto LD, Correa A, Erickson JD. 2001. Racial and temporal variations in the prevalence of heart defects. Pediatrics 107: E32. Bruns D. 2011. 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Human malformations and related anomalies, 2e. Oxford: University Press. Sugayama SMM, Kim CA, Albano LMJ, Utagawa CY, Bertola DR, Koiffmann CP, Gonzalez CH. 1999. Estudo genético-clínico de 20 pacientes com trissomia 13 (síndrome de Patau). Pediatria (São Paulo) 21: 21– 29. Wyllie JP, Wright MJ, Burn J, Hunter S. 1994. Natural history of trisomy 13. Arch Dis Child 71: 343– 345. Yukifumi M, Hirohiko S, Fukiko I, Mariko M. 2011. Trisomy 13 in a 9-year-old girl with left ventricular noncompaction. Pediatr Cardiol 32: 206– 207. Zen PRG, Rosa RFM, Rosa RCM, Dale Mulle L, Graziadio C, Paskulin GA. 2008. Aspectos clínicos não usuais de pacientes portadores da síndrome de Patau e Edwards: um desafio diagnóstico? Rev Paul Ped 26: 295– 299. Citing Literature Volume164, Issue1January 2014Pages 272-275 ReferencesRelatedInformation
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