Total: 6 |
|
PMID (PMCID) | ||
---|---|---|
31181251 |
OTHER | |
Fetal methotrexate syndrome: A systematic review of case reports. | ||
Verberne EA, de Haan E, van Tintelen JP, Lindhout D, van Haelst MM. Reprod Toxicol. 2019;87:125-139. |
||
Statistically significant higher proportions of microcephaly, craniosynostosis, tetralogy of Fallot, pulmonary valve atresia, limb reduction defects and syndactyly were found in the methotrexate group, indicating that these congenital anomalies are truly part of the fetal methotrexate syndrome. | ||
7818335 |
FEMALE | Child |
Tetralogy of Fallot with anomalous origin of the right coronary artery. | ||
Moss RL, Backer CL, Zales VR, Florentine MS, Mavroudis C. Ann Thorac Surg. 1995;59(1):229-31. |
||
This report describes a child with tetralogy of Fallot and acquired pulmonary valve atresia in whom the pulmonary blood flow was provided solely by retrograde flow from an anomalous right coronary artery originating from the main pulmonary artery. | ||
1396843 |
FEMALE | |
Laser-assisted tricuspid valve balloon dilation for acquired tricuspid valve atresia. | ||
Rosenthal E, Kakadekkar AP, Qureshi SA, Tynan M. Eur Heart J. 1992;13(9):1296-8. |
||
Acquired pulmonary valve atresia is a well-recognized but uncommon complication of surgical systemic-to-pulmonary artery shunts in patients with tetralogy of Fallot. | ||
1845646 |
MIXED_SAMPLE | Infant, Newborn |
[Di George syndrome]. | ||
Urrejola P, Cattani A, Heusser F, Talesnik E. Rev Chil Pediatr. 1991;62(6):381-5. |
||
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). | ||
4003436 |
MIXED_SAMPLE | Child |
Tetralogy of Fallot with pulmonary atresia in siblings. | ||
Der Kaloustian VM, Ratl H, Malouf J, Hatem J, Slim M, Tomeh A, Khouri J, Kutayli F. Am J Med Genet. 1985;21(1):119-22. |
||
We present two sisters with tetralogy of Fallot and pulmonary valve atresia. | ||
6698063 |
MALE | Infant |
Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival. | ||
Winter WE, Silverstein JH, Barrett DJ, Kiel E. Eur J Pediatr. 1984;141(3):171-2. |
||
Two brothers with DiGeorge syndrome had tetralogy of Fallot with pulmonary valve atresia, illustrating similarity of the type of congenital heart disease (CHD) within affected families; the specific type of CHD differs between families. |