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Journal of Obstetrics and Gynaecology Volume 30, 2010 - Issue 6
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Obstetric Case Reports

Trisomy 22: The heart aspect

E. N. Kontomanolisa EGA/OH, UCLH, Department of Fetal Medicine, London, UKCorrespondence[email protected]
,
P. Pandyaa EGA/OH, UCLH, Department of Fetal Medicine, London, UK
&
V. Limperisb Department of Obstetrics and Gynaecology, Democritus University, Alexandroupolis, Greece
Pages 627-628 | Published online: 11 Aug 2010

References

  • Allotey J, Lacaille F, Lees MM, et al 2008. Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidy. Journal of Pediatric Surgery 43:1736–1740.
  • Bacino CA, Schreck R, Fischel-Ghodsian N, et al 1995. Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature. American Journal of Medical Genetics 56:359–365.
  • Hall T, Samuel M, Brain J. 2009. Mosaic trisomy 22 associated with total colonic aganglionosis and malrotation. Journal of Pediatric Surgery 44:e9–e11.
  • McPherson E, Stetka DG. 1990. Trisomy 22 in a liveborn infant with multiple congenital anomalies. American Journal of Medical Genetics 36:11–14.
  • Mokate T, Leask K, Mehta S, et al 2006. Non-mosaic trisomy 22: a report of 2 cases. Prenatal Diagnosis 26:962–965.
  • Stoll C, Medeiros P, Pecheur H, et al 1997. De novo trisomy 22 due to an extra 22Q-chromosome. Annals of Genetics 40:217–221.
  • Thomas S, Parker M, Tan J, et al 2004. Ocular manifestations of mosaic trisomy 22: a case report and review of the literature. Ophthalmic Genetics 25:53–56.
  • Van Buggenhout GJ, Verbruggen J, Fryns JP. 1995. Renal agenesis and trisomy 22: a case report and review. Annals of Genetics 38:44–48.

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