Pulmonary atresia with ventricular septal defect: Prevalence of deletion 22q11 in the different anatomic patterns

Italian Heart Journal

Volumn 2, Issue 5, 2001, Pages 384-387

  Anaclerio, S ^a   Marino, B ^a   Carotti, A ^a   Digilio, M C ^a   Toscano, A ^a   Gitto, P ^a   Giannotti, A ^a   Di Donato, R ^a   Dallapiccola, B ^a  

^a Divisione di Cardiologia   (Italy)

Author keywords

Congenital heart disease; Deletion 22q11; Genetics

Indexed keywords

ANATOMY; AORTA; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; COLLATERAL CIRCULATION; CONTROLLED STUDY; DIGEORGE SYNDROME; DISEASE ASSOCIATION; FEMALE; GENETIC DISORDER; GREAT VESSELS TRANSPOSITION; HEART DISEASE; HEART LEFT VENTRICLE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; LUNG ATRESIA; LUNG CIRCULATION; MAJOR CLINICAL STUDY; MALE; MORPHOGENESIS; NEWBORN; PREVALENCE; PULMONARY ARTERY; TRICUSPID VALVE ATRESIA; VELOCARDIOFACIAL SYNDROME;

CHILD WELFARE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FAMILY HEALTH; FEMALE; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INFANT; INFANT WELFARE; INFANT, NEWBORN; LUNG; MALE; PREVALENCE; PULMONARY ATRESIA;

EID: 0034976020     PISSN: 1129471X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

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2. Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia
3. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion
4. Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect
5. Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries
6. Spectrum of clinical features associated with interstitial chromosome 22q11 deletion: A European collaborative study
7. Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome
8. Frequency of 22q11 deletion in patients with conotruncal defects
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10. Patterns of pulmonary arterial anatomy and blood supply in complex congenital heart disease with pulmonary atresia
11. Total repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collaterals: An integrated approach
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13. Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot
14. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome
15. Deletion 22q11 in patients with interrupted aortic arch
16. Congenital heart surgery nomenclature and database project: Pulmonary atresia-ventricular septal defect
17. Chromosome 22q11 microdeletion and congenital heart disease. A survey in a pediatric population
18. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: No evidence for deletion in non syndromic patients
19. 22q11.2 deletions in a series of patients with non selective congenital heart defects: Incidence, type of defects and parental origin