Conotruncal heart malformations
MONDO:0016581Conotruncal heart malformations are a group of congenital cardiac outflow tract anomalies that include such defects as tetralogy of Fallot, pulmonary atresia with ventricular septal defect, double-outlet right ventricle (DORV), double-outlet left ventricle, truncus arteriosus and transposition of the great arteries (TGA), among others. This group of defects is frequently found in patients with 22q11.2 deletion syndrome. A deletion of chromosome 22q11.2 has equally been associated in a subset of patients with various types of isolated non-syndromic conotruncal heart malformations (with the exception of DORV and TGA where this is very uncommon).
Also known as: Taussig-Bing syndrome or defect, conotruncal heart malformations, conotruncal heart malformations, variable, CTHM, Double-outlet right ventricle, conotruncal anomaly face syndrome, conotruncal cardiac defects, interrupted aortic Arch
41 clinical trials for this condition and its sub-types, 1 tagged with Conotruncal heart malformations itself.
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Browse by category →Sub-types of Conotruncal heart malformations
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Tetralogy of fallot 33 trials
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Persistent truncus arteriosus 8 trials
2 sub-types
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Double outlet right ventricle 2 trials · 3 incl. sub-types
5 sub-types
- Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis 1 trial
- Double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy 0 trials
- Double outlet right ventricle with non-committed subpulmonary ventricular septal defect 0 trials
- Double outlet right ventricle with subaortic or doubly committed ventricular septal defect 0 trials
- Double outlet right ventricle with subpulmonary ventricular septal defect 0 trials
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3 sub-types
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Congenital aortopulmonary window 0 trials
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Double outlet left ventricle 0 trials
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Pulmonary valve agenesis 0 trials