Tetralogy of Fallot

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Pulmonic stenosis

A narrowing of the right ventricular outflow tract that can occur at the pulmonary valve (valvular stenosis) or just below the pulmonary valve (infundibular stenosis).


Total: 12

                       


(per page)
PMID (PMCID)
18773675
 MALE Infant
Tetralogy of Fallot and hypertrophic cardiomyopathy in a case of cardiofaciocutaneous syndrome.
Yildirim SV, Kale-Cekinmez E, Ozcan D, Derbent M.
Turk J Pediatr. 2008;50(3):275-7.
Pulmonic stenosis, atrial and ventricular septal defects, patent ductus arteriosus, and hypertrophic cardiomyopathy are cardiac findings identified in patients with this syndrome; however, tetralogy of Fallot has never been associated with CFC syndrome.
17215642
 MALE
Uncorrected tetralogy of Fallot in an 86-year-old patient.
Alonso A, Downey BC, Kuvin JT.
Am J Geriatr Cardiol. 2007;16(1):38-41.
Transthoracic and transesophageal echocardiography revealed infundibular pulmonic stenosis with a ventricular septal defect, overriding aorta, and right ventricular hypertrophy, findings consistent with unrepaired tetralogy of Fallot.
11484200
 MIXED_SAMPLE Infant, Newborn
Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
Leonardi ML, Pai GS, Wilkes B, Lebel RR.
Am J Med Genet. 2001;102(3):237-42.
Cardiac manifestations include ventricular septal defect, atrial septal defect, tetralogy of Fallot, double outlet right ventricle, hypoplastic left heart, aortic stenosis, pulmonic stenosis and other valvular anomalies.
11593211
 MIXED_SAMPLE Infant, Newborn
Unusual echocardiographic views of bicuspid and tricuspid pulmonic valves.
McAleer E, Kort S, Rosenzweig BP, Katz ES, Tunick PA, Phoon CK, Kronzon I.
J Am Soc Echocardiogr. 2001;14(10):1036-8.
Bicuspid pulmonic valve is one cause of pulmonic stenosis, which is especially common in tetralogy of Fallot.
10213047
 MIXED_SAMPLE
Jagged1 mutations in patients ascertained with isolated congenital heart defects.
Krantz ID, Smith R, Colliton RP, Tinkel H, Zackai EH, Piccoli DA, Goldmuntz E, Spinner NB.
Am J Med Genet. 1999;84(1):56-60.
Most commonly these are right-sided defects ranging from mild peripheral pulmonic stenosis to severe forms of tetralogy of Fallot.
10213047
 MIXED_SAMPLE
Jagged1 mutations in patients ascertained with isolated congenital heart defects.
Krantz ID, Smith R, Colliton RP, Tinkel H, Zackai EH, Piccoli DA, Goldmuntz E, Spinner NB.
Am J Med Genet. 1999;84(1):56-60.
This leads us to hypothesize that defects in Jagged1 can be found in patients with presumably isolated heart defects, such as tetralogy of Fallot or pulmonic stenosis.
8985486
 FEMALE Infant, Newborn
Distichiasis-lymphedema syndrome: tetralogy of Fallot, chylothorax, and neonatal death.
Chen E, Larabell SK, Daniels JM, Goldstein S.
Am J Med Genet. 1996;66(3):273-5.
Subsequent to surgery for tetralogy of Fallot, patent ductus arteriosus, and branch pulmonic stenosis, she developed persistent chylothorax and sepsis.
2968045
 FEMALE Adult
Fetal cardiac Doppler flow studies in prenatal diagnosis of heart disease.
Shenker L, Reed KL, Marx GR, Donnerstein RL, Allen HD, Anderson CF.
Am J Obstet Gynecol. 1988;158(6 Pt 1):1267-73.
We present six cases in which Doppler studies contributed to the accuracy of the diagnosis of fetal heart disease, including tetralogy of Fallot, right and left ventricular hypoplasia, atrioventricular canal defect, double-outlet right ventricle, and pulmonic stenosis.
650896
 MALE Child
Quantitative angiocardiographic recognition of atypical form of tetralogy of Fallot with absent pulmonic valve.
Yazdanyar A, Safavian MH, Nazarian I, Shakibi JG.
Jpn Heart J. 1978;19(1):167-73.
The lack of the usual manifestations of tetralogy of Fallot with absent pulmonic valve was due to supravalvar pulmonic stenosis, acting as a natural pulmonary artery band.
650896
 MALE Child
Quantitative angiocardiographic recognition of atypical form of tetralogy of Fallot with absent pulmonic valve.
Yazdanyar A, Safavian MH, Nazarian I, Shakibi JG.
Jpn Heart J. 1978;19(1):167-73.
It is concluded that a quantitative evaluation of the ratio of the transverse diameter of the main pulmonary artery to the aortic root on lateral angiocardiogram allows differentiation of tetralogy of Fallot with absent pulmonic valve associated with supravalvular pulmonic stenosis from uncomplicated forms of tetralogy of Fallot.
650896
 MALE Child
Quantitative angiocardiographic recognition of atypical form of tetralogy of Fallot with absent pulmonic valve.
Yazdanyar A, Safavian MH, Nazarian I, Shakibi JG.
Jpn Heart J. 1978;19(1):167-73.
A 9-year-old boy is reported who had tetralogy of Fallot, rudimentary pulmonic valve, and supravalvar pulmonic stenosis.
650896
 MALE Child
Quantitative angiocardiographic recognition of atypical form of tetralogy of Fallot with absent pulmonic valve.
Yazdanyar A, Safavian MH, Nazarian I, Shakibi JG.
Jpn Heart J. 1978;19(1):167-73.
It is concluded that a quantitative evaluation of the ratio of the transverse diameter of the main pulmonary artery to the aortic root on lateral angiocardiogram allows differentiation of tetralogy of Fallot with absent pulmonic valve associated with supravalvular pulmonic stenosis from uncomplicated forms of tetralogy of Fallot.