J Korean Soc Neonatol.  2007 Nov;14(2):237-242.

A Case of Addition of Chromosome 3 associated with Multiple Anomalies

Affiliations
  • 1Department of Pediatrics, School of Medicine, Catholic University of Daegu, Daegu, S. Korea. wootykim@cu.ac.kr
  • 2Department of Opthalmology, Dongguk University College of Medicine, Gyeongju, S. Korea.

Abstract

Chromosomal anomalies are associated with various congenital malformations and impaired development. The addition or duplication of chromosome 3 is a very rare chromosomal anomaly, in comparison to the deletion of chromosome 3. To date, only one case of the duplication of chromosome 3p has been reported, but an addition or duplication of chromosome 3p was not reported in Korea. We experienced a case of the addition of chromosome 3 in a male newborn infant who had suffered from multiple anomalies and congenital heart disease, atrioventricular septal defects and coarctation of the aorta. The karyotype of this patient was 46, XY, add(3)(p25). We report the case with the review of the associated literatures.

Keyword

Addition; Duplication; Chromosome 3; Anomaly

MeSH Terms

Aortic Coarctation
Chromosomes, Human, Pair 3*
Heart Defects, Congenital
Humans
Infant, Newborn
Karyotype
Korea
Male
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