A Case of Addition of Chromosome 3 associated with Multiple Anomalies
Journal of the Korean Society of Neonatology
;
: 237-242, 2007.
Article
Dans Coréen
| WPRIM
| ID: wpr-148550
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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Coarctation aortique
/
Chromosomes humains de la paire 3
/
Caryotype
/
Cardiopathies congénitales
/
Corée
Limites du sujet:
Humains
/
Mâle
/
Nouveau-né
Pays comme sujet:
Asie
langue:
Coréen
Texte intégral:
Journal of the Korean Society of Neonatology
Année:
2007
Type:
Article
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS