合計: 4 |
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PMID (PMCID) | ||
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25593538 |
FEMALE | Infant, Newborn |
Importance of absent ductus arteriosus in tetralogy of Fallot with absent pulmonary valve syndrome. | ||
Qureshi MY, Burkhart HM, Julsrud P, Cetta F. Tex Heart Inst J. 2014;41(6):664-7. |
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Both patients had a combination of tetralogy of Fallot with absent pulmonary valve syndrome and right aortic arch with retroesophageal left subclavian artery without a vascular ring. | ||
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. |
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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. | ||
1845646 |
MIXED_SAMPLE | Infant, Newborn |
[Di George syndrome]. | ||
Urrejola P, Cattani A, Heusser F, Talesnik E. Rev Chil Pediatr. 1991;62(6):381-5. |
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Their main clinical symptoms were hypocalcemic convulsions, unusual facies (hyperthelorism, low set prominent ears, micrognathia, short philtrum) and cardiac malformations (vascular ring with right aortic arc, aberrant left innominated artery and ligamentum arteriosus in one of them and Tetralogy of Fallot with pulmonary valve atresia in the other). | ||
3628069 |
MIXED_SAMPLE | Infant |
Surgical management in tetralogy of Fallot and vascular ring. | ||
Virdi IS, Keeton BR, Shore DF, Monro JL. Pediatr Cardiol. 1987;8(2):131-4. |
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The management of three infants born with a combination of tetralogy of Fallot and a vascular ring causing tracheoesophageal compression is described. |