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.

Tracheomalacia



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PMID (PMCID)
7899124
 MIXED_SAMPLE Infant, Newborn
Pediatric intrathoracic large airway obstruction: diagnostic and therapeutic considerations.
Sagy M, Silver P, Nimkoff L, Zahtz G, Amato JJ, Bierman FZ.
Pediatr Emerg Care. 1994;10(6):351-8.
The patients were a four month old with bronchial cartilage hypoplasia presenting as congenital lobar emphysema; a one month old with segmental bronchomalacia; a one month old with tracheal bronchus; a two day old and a seven month old with aneurysmal distension of the pulmonary arteries secondary to tetralogy of Fallot, with absent pulmonary valve and atrioventricular canal with pulmonary poststenotic dilatation, respectively; a three year old with double aortic arch forming a vascular ring; and a three month old with tracheomalacia from tracheoesophageal fistula.
8456824
 FEMALE Infant, Newborn
Fryns syndrome.
Stratton RF, Young RS, Heiman HS, Carter JM.
Am J Med Genet. 1993;45(5):562-4.
She also had a unilateral cleft lip, camptodactyly, duodenal atresia, tracheomalacia, bronchomalacia, and Tetralogy of Fallot.