Cardiovascular anomalies associated with chromosome 22q11.2 deletion

International Journal of Cardiology

Volumn 114, Issue 2, 2007, Pages 147-149

  Momma, Kazuo ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACCESSORY SPLEEN; AORTA ARCH INTERRUPTION; AORTA COARCTATION; AORTA VALVE DISEASE; AORTA VALVE STENOSIS; ARTERIAL TRUNK; CARDIOVASCULAR MALFORMATION; CHROMOSOME 21Q; CHROMOSOME DELETION; CORRELATION ANALYSIS; DISEASE ASSOCIATION; EDITORIAL; FALLOT TETRALOGY; GREAT VESSELS TRANSPOSITION; HEART ATRIUM SEPTUM DEFECT; HEART RIGHT VENTRICLE DOUBLE OUTLET; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; LUNG ATRESIA; LUNG VEIN DRAINAGE ANOMALY; PATENT DUCTUS ARTERIOSUS; PREVALENCE; PRIORITY JOURNAL; PULMONARY VALVE ATRESIA; PULMONARY VALVE STENOSIS; TRICUSPID VALVE ATRESIA;

BLOOD VESSELS; CHROMOSOMES, HUMAN, PAIR 22; GENE DELETION; HEART DEFECTS, CONGENITAL; HUMANS;

EID: 33751201822     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2006.02.002     Document Type: Editorial

References (12)

1. Johnson M.C., and Strauss A.W. Genetic control in pediatric cardiovascular medicine. In: Moller J.H., and Hoffman J.I.C. (Eds). Pediatric cardiovascular medicine (2000), Churchill Livingstone, New York 21-34
2. Momma K., Takao A., Matsuoka R., et al. Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults. Genet Med 3 (2001) 56-60
3. Park I.-S., Ko J.-K., Kim Y.-H., et al. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study. Int J Cardiol 114 (2006) 230-235 10.1016/j.ijcard.2005.12.029 [this issue]
4. Baravelli M., Borghi A., Rogiani S., et al. Clinical, anatomopathological and genetic pattern of 10 patients with cervical aortic arch. Int J Cardiol 114 (2006) 236-240 10.1016/j.ijcard.2005.12.028 [this issue]
5. Matsuoka R., Kimura M., Scambler P.J., et al. Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome. Hum Genet 103 (1998) 70-80
6. Ryan A.K., Goodship J.A., Wilson D.I., et al. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet 34 (1997) 798-804
7. Marino B., Digilio M.C., Toscano A., et al. Anatomic patterns of conotruncal defects associated with deletion 22q11. Genet Med 3 (2001) 45-48
8. Momma K., Kondo C., and Matsuoka R. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion. J Am Coll Cardiol 27 (1996) 198-202
9. Boudjemline Y., Fermont L., Le Bidois J., et al. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study. J Pediatr 138 (2001) 520-524
10. Beauchesne L.M., Warnes C.A., Connolly H.M., et al. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies. J Am Coll Cardiol 45 (2005) 595-598
11. Momma K., Kondo C., Ando M., et al. Tetralogy of Fallot associated with chromosome 22q11 deletion. Am J Cardiol 76 (1995) 618-621
12. Momma K., Kondo C., Matsuoka R., et al. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome. Am J Cardiol 78 (1996) 591-594