Results 61 to 70 of about 1,273 (168)
Pediatric Investigation, Volume 8, Issue 4, Page 287-294, December 2024.Gastrointestinal complications are common perioperative complications in children with congenital heart disease, and as near‐infrared reflectance spectroscopy (NIRS) provides a non‐invasive, real‐time monitoring of regional tissue oxygenation, we envisioned monitoring and preventing the development of gastrointestinal complications through the use of ...
Wenpeng Xie +4 more
wiley +1 more source
Use of an autologous pericardial patch to repair a post‐traumatic caudal vena cava cicatrix in a dog
Veterinary Surgery, Volume 53, Issue 8, Page 1455-1460, November 2024.Abstract Objective To report the use of a pericardial patch graft to repair a post‐traumatic caudal vena cava cicatrix in a dog. Study design Case report. Animals A 1 year‐old Rottweiler presenting with ascites following presumed blunt thoracic trauma.
Joshua M. Winter +2 more
wiley +1 more source
Updated EUROCAT guidelines for classification of cases with congenital anomalies
Birth Defects Research, Volume 116, Issue 2, February 2024.Abstract Background Precise and correct classification of congenital anomalies is important in epidemiological studies, not only to classify according to etiology but also to group similar congenital anomalies together, to create homogeneous subgroups for surveillance and research.
Jorieke E. H. Bergman +7 more
wiley +1 more source
Clinical Case Reports, Volume 12, Issue 1, January 2024.Key Clinical Message Ectopia cordis is a rare condition with expected low survival rate based on past studies. We encountered a case of a preterm and low birth weight infant with ectopia cordis. When the infant cried, the prolapse of the heart, liver, and intestinal tract worsened. A pressure‐applying protector was used to protect the organs and reduce
Takeo Mukai +7 more
wiley +1 more source
Cor triatriatum dexter: A rare cause of childhood cyanosis
Annals of Pediatric Cardiology, 2012 Cor triatriatum dexter is a rare congenital heart anomaly where the right atrium is divided into two chambers by a membrane. We report a boy who had persistent mild cyanosis and diagnosed to have cor triatriatum dexter with secundum atrial septal defect ...
Ahmad Rustam bin Mohd Zainudin +2 more
doaj +1 more source
Different Cardiac Anomalies in Mother and Son with 4q-Syndrome
Case Reports in Genetics, 2015 We report a female patient with asymptomatic cor triatriatum sinister, associated with 4q34.3 deletion. Her child, carrying the same imbalance, suffers from tetralogy of Fallot.
Marcello Marcì +3 more
doaj +1 more source
Radiology Case ReportsCor triatriatum is an uncommon cardiac defect that occurs in 0.1-0.4% of congenital heart disease patients. It is characterized by a fibromuscular membrane separating the left (sinister) or the right (Dexter) atriums in tow chambers.
Yunis Daralammouri, MD +2 more
doaj +1 more source
Standard Poster Abstracts for the 17th Asia Pacific Heart Rhythm Society (APHRS) Scientific Sessions
Journal of Arrhythmia, Volume 41, Issue 2, April 2025.
wiley +1 more source