Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome - 11/09/11
Doi : 10.1016/S0002-9149(96)00374-8
Kazuo Momma, MD 1, Chisato Kondo, MD, Rumiko Matsuoka, MD, Atsuyoshi Takao, MD
From the Department of Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical College, Tokyo, Japan
Abstract |
Cardiac anomalies associated with a chromosome 22q11 deletion are typically Tetralogy of Fallot complicated with anomalies of the aortic arch, ductus arteriosus, and pulmonary artery.
Le texte complet de cet article est disponible en PDF. | This study was supported by grants from the Japan Research Promotion Society for Cardiovascular Diseases, the Ministry of Health and Welfare, the Ministry of Education, the Japan Ship Foundation, a grant from Takeda Science Foundation, and Japan Private School Promotion Foundation. |
© 1996
Publié par Elsevier Masson SAS.
Vol 78 - N° 5
P. 591-594 - septembre 1996 Retour au numéro
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