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Monozygotic twins with chromosome 22q11 microdeletion and discordant phenotypes in cardiovascular patterning.
- Source :
-
Pediatric cardiology [Pediatr Cardiol] 2001 May-Jun; Vol. 22 (3), pp. 260-3. - Publication Year :
- 2001
-
Abstract
- Monozygotic twins with chromosome 22q11 microdeletions offer an ideal situation to observe the association of microdeletion and disrupted cardiovascular patterning. We report monozygotic twins concordant for 22q11.2 microdeletion but discordant for cardiovascular patterning. Both twins showed identical intracardiac defects including tetralogy of Fallot with pulmonary atresia. Nevertheless, their great vessel patternings were variable. These twins show that the mispatterning of the great vessels may not correlate with intracardiac morphogenesis. The discordant development of the great vessels, especially in the pulmonary vascular system, has clinical significance for prognosis. The phenotypic variability of cardiovascular anomalies seen in 22q11 microdeletion cannot be explained on the basis of genotypic difference.
- Subjects :
- Chromosomes, Human, Pair 22 genetics
Female
Humans
Infant, Newborn
Neural Crest embryology
Phenotype
Pulmonary Atresia genetics
Sequence Deletion genetics
Tetralogy of Fallot genetics
Twins, Monozygotic
Abnormalities, Multiple genetics
Diseases in Twins embryology
Diseases in Twins genetics
Heart Defects, Congenital embryology
Heart Defects, Congenital genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0172-0643
- Volume :
- 22
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Pediatric cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 11343161
- Full Text :
- https://doi.org/10.1007/s002460010219