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Tetracuspid aortic valve in a patient with 22q11.2 microdeletion

2000; Wiley; Volume: 93; Issue: 1 Linguagem: Inglês

10.1002/1096-8628(20000703)93

1096-8628

Masao Nakagawa, Nobuhiko Okamoto, Hidetoshi Fujino, Noriko Watanabe, Masahiko Okuno,

Coronary Artery Anomalies

American Journal of Medical GeneticsVolume 93, Issue 1 p. 74-75 Letter to the Editor Tetracuspid aortic valve in a patient with 22q11.2 microdeletion Masao Nakagawa, Corresponding Author Masao Nakagawa [email protected] Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanDepartment of Pediatrics, Shiga University of Medical Science, Seta, Otsu, Shiga 520-2192, JapanSearch for more papers by this authorNobuhiko Okamoto, Nobuhiko Okamoto Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanSearch for more papers by this authorHidetoshi Fujino, Hidetoshi Fujino Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanSearch for more papers by this authorNoriko Watanabe, Noriko Watanabe Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanSearch for more papers by this authorMasahiko Okuno, Masahiko Okuno Department of Pediatrics, Nagahama Red Cross Hospital, Nagahama, JapanSearch for more papers by this author Masao Nakagawa, Corresponding Author Masao Nakagawa [email protected] Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanDepartment of Pediatrics, Shiga University of Medical Science, Seta, Otsu, Shiga 520-2192, JapanSearch for more papers by this authorNobuhiko Okamoto, Nobuhiko Okamoto Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanSearch for more papers by this authorHidetoshi Fujino, Hidetoshi Fujino Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanSearch for more papers by this authorNoriko Watanabe, Noriko Watanabe Department of Pediatrics, Shiga University of Medical Science, Otsu, JapanSearch for more papers by this authorMasahiko Okuno, Masahiko Okuno Department of Pediatrics, Nagahama Red Cross Hospital, Nagahama, JapanSearch for more papers by this author First published: 12 June 2000 https://doi.org/10.1002/1096-8628(20000703)93:1 3.0.CO;2-PCitations: 3Read 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 Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES Fokstuen S, Arbenz U, Artan S, Bauersfeld U, Brecevic L, Fasnacht M, Rothlisberger B, Schinzel A. 1998. 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin. Clin Genet 53: 63–69. Kazuma N, Murakami M, Suzuki Y, Umezu R, Murata M. 1997. Cervical aortic arch associated with 22q11.2 deletion. Pediatr Cardiol 18: 149–151. Kirby ML, Gale TF, Stewart DE. 1983. Neural crest cells contribute to aorticopulmonary septation. Science 220: 1059–1061. Nishibatake M, Kirby ML, Van Mierop LHS. 1987. Pathogenesis of persistent truncus arteriosus and dextroposed aorta in the chick embryo after neural crest ablation. Circulation 75: 255–264. Payne RM, Johnson MC, Grant JW, Strauss AW. 1995. Toward a molecular understanding of congenital heart disease. Circulation 91: 494–504. Citing Literature Volume93, Issue13 July 2000Pages 74-75 ReferencesRelatedInformation