Dextrocardia with sinus solitus
- Giant left atrium and a right sided heart. Nigri, M.; Fernandes, J. L.; Rochitte, C. E. // Heart;Apr2007, Vol. 93 Issue 4, p475
An image is presented of human abnormalities in the heart.
- atelocardia. // Taber's Cyclopedic Medical Dictionary (2009);2009, Issue 21, p207
A definition of the medical term "atelocardia," which refers to a congenital incomplete development of the heart, is presented.
- A New Anomaly at the Center of the Heart? Angelini, Paolo // Texas Heart Institute Journal;1999, Vol. 26 Issue 4, p249
Editorial. Comments on an article by C.L. Birincioglu and colleagues about an unclassified cardiac anomaly. How cardiac anomalies should be studied; Features of the cardiac defect in question; Treatment for the anomaly.
- Riluzole. // Reactions Weekly;10/20/2012, Issue 1424, p45
The article describes the case of a male fetus who developed intrauterine growth restriction and was born with cardiac malformation after in utero exposure to riluzole used by his 38-year-old mother for treating amyotrophic lateral sclerosis.
- Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland. Wozniak, Anna; Wolnik-Brzozowska, Danuta; Wisniewska, Marzena; Glazar, Renata; Materna-Kiryluk, Anna; Moszura, Tomasz; Badura-Stronka, Magdalena; Skolozdrzy, Joanna; Krawczynski, Maciej R.; Zeyland, Joanna; Bobkowski, Waldemar; Slomski, Ryszard; Latos-Bielenska, Anna; Siwinska, Aldona // BMC Pediatrics;2010, Vol. 10, p88
Background: The 22q11.2 microdeletion syndrome (22q11.2 deletion syndrome -22q11.2DS) refers to congenital abnormalities, including primarily heart defects and facial dysmorphy, thymic hypoplasia, cleft palate and hypocalcaemia. Microdeletion within chromosomal region 22q11.2 constitutes the...
- CardiopatÃa CongÃ©nita en Autopsia de NiÃ±os con SÃndrome de Down. González-Ramos, Luis Antonio; Martínez-Carballo, Erika Matilde; Rascón-Alcantar, Adela // Boletin Clinico Hospital Infantil del Estado de Sonora;Apr2013, Vol. 30 Issue 1, p39
Congenital heart disease in Down syndrome is common. We present the findings of congenital heart disease in autopsies of children who died of various causes at the Sonora Children's Hospital in the period 1978-2012, it was found that the group of complex malformations was the most frequent...
- Splenopancreatic Field Abnormality Is Not Unique to Trisomy 13. Perez, Luiz Cesar; Henrique, Gustavo; Barbosa, T. De Sales; Careta, Renata Scarpat; Nassif, Cristiane Miziara; de Pina-Neto, João Monteiro; Giuliani, Liane R.; Martinhago, Ciro Dresch; Gomy, Israel // Pediatric & Developmental Pathology;Jan/Feb2004, Vol. 7 Issue 1, p91
Splenopancreatic fusion is an uncommon finding, usually only seen as part of the splenopancreatic field abnormality associated with trisomy 13. It may present itself either as ectopic splenic tissue in the cauda pancreatis, as ectopic pancreatic tissue in the spleen or accessory spleen, or as...
- Socioeconomic Status in Relation to Selected Birth Defects in a Large Multicentered US Case-Control Study. J. Yang; S. L. Carmichael; M. Canfield; J. Song; G. M. Shaw; the National Birth Defects Prevention Study // American Journal of Epidemiology;Jan2008, Vol. 167 Issue 2, p145
This study examined individual and household socioeconomic status (SES) in relation to phenotypes of neural tube defects, orafacial clefts, and conotruncal heart defects using data from the National Birth Defects Prevention Study with 2,551 nonmalformed liveborn controls and 1,841 cases...
- AsociaciÃ³n VACTER: reporte de un caso. Rodríguez Z., Eréndira; Firó R., Verónica; Peláez, Aarón; Pedroza M., J. Manuel // Revista Mexicana de Pediatria;May/Jun2013, Vol. 80 Issue 3, p109
VACTER association is described as the set of congenital anomalies that may present a single patient: vertebral defects, anal defects, cardiac malformations, tracheal esophageal fistula and radial and renal anomalies. Generally, brain development is normal as there is no central nervous system...