Isolated innominate artery in 22q11 microdeletion

Pediatric Cardiology

Volumn 22, Issue 1, 2001, Pages 80-82

  Duke, C ^a   Chan, K C ^a  

^a GLENFIELD HOSPITAL   (United Kingdom)

Author keywords

22q11 deletion; Aortic arch anomaly; Cervical aortic arch; DiGeorge syndrome; Isolated innominate artery

Indexed keywords

AORTA ARCH ANOMALY; ARTICLE; BRACHIOCEPHALIC TRUNK; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; DIGEORGE SYNDROME; ECHOCARDIOGRAPHY; FALLOT TETRALOGY; HEART CATHETERIZATION; HEART RIGHT VENTRICLE OUTFLOW TRACT; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYPOCALCEMIA; INFANT; LYMPHOCYTE COUNT; MALE; PREMATURITY; PULMONARY VALVE STENOSIS; THORAX RADIOGRAPHY;

BRACHIOCEPHALIC TRUNK; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FATAL OUTCOME; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INFANT, NEWBORN; MALE; TETRALOGY OF FALLOT;

EID: 0035123119     PISSN: 01720643     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002460010163     Document Type: Article

References (10)

1. Coarctation of the aorta with right aortic arch and isolation of the left innominate artery: A surgical challenge in a patient without collateral posterior brain circulation
2. Anomalies of the derivatives of the aortic arch system
3. Right aortic arch with aberrant left innominate artery
4. Isolation of the left brachiocephalic artery associated with right aortic arch and left sided arterial duct
5. Tetralogy of Fallot associated with chromosome 22q11 deletion
6. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion
7. Right aortic arch with aberrant retroesophageal innominate artery: A report of 2 cases and review of the literature
8. Isolation of a subclavian artery
9. Isolated innominate artery in asplenia syndrome with aorticatresia: Newly recognised cardiovascular complex
10. A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects