Results 81 to 90 of about 4,976 (217)
Genetic testing for Ebstein anomaly
Ebstein anomaly (EA) is a rare congenital tricuspid valve malformation, characterized by downward displacement of the septal leaflet and an atrialized right ventricle.
Rakhmanov Yeltay +5 more
doaj +1 more source
Functional pulmonary atresia is characterized by a structurally normal pulmonary valve that does not open during right ventricular ejection. It is usually associated with Ebstein′s anomaly, Uhl′s anomaly, neonatal Marfan syndrome and tricuspid valve ...
Gürkan Altun +4 more
doaj +1 more source
Zero Fluoroscopy Ablation of Arrhythmias in Patients With Congenital Heart Disease
Zero‐fluoroscopy radiofrequency ablation using 3D electroanatomic mapping was performed in 42 patients with mild, moderate, or great complexity congenital heart disease. Acute success was 100%, with no complications and minimal recurrence over 48 months. This approach eliminates radiation exposure while maintaining safety and efficacy across select yet
Shailendra Upadhyay +4 more
wiley +1 more source
ABSTRACT We present a 74‐year‐old female with a history of mechanical aortic and mitral valve implantation and non‐Hodgkin lymphoma. She presented with right sided heart failure due to severe functional tricuspid regurgitation and was treated with transcatheter TricValve bicaval system implantation.
Marcel A. Beijk +2 more
wiley +1 more source
Demonstration of circular shunt in fetal Ebstein anomaly
Ebstein′s anomaly was diagnosed in a fetus at 24 weeks of gestation. There was significant cardiomegaly and severe tricuspid regurgitation (TR). There was functional pulmonary atresia with severe pulmonary regurgitation (PR) and this was causing a ...
Deepa Sasikumar +2 more
doaj +1 more source
Left ventricular hypertrabeculation/noncompaction with epilepsy, other heart defects, minor facial anomalies and new copy number variants [PDF]
BACKGROUND: Left ventricular hypertrabeculation/noncompaction (LVHT) is a cardiac abnormality of unknown etiology which has been described in children as well as in adults with and without chromosomal aberrations.
Bert Nagel +5 more
core +1 more source
ABSTRACT While the standard diagnostic test for suspected 22q copy number disorders is by chromosomal microarray, this case highlights the importance of utilizing FISH to localize allelic copy number when there is a family history of deletion/duplication syndrome for accurate recurrence risk assessment.
Laura M. Bryant +5 more
wiley +1 more source
Background Once surgical management is indicated, variation of Ebstein valve morphology affects surgical strategy. This study explored practical, easily measureable, cardiovascular magnetic resonance (CMR)-derived attributes that may contribute to the ...
Marina L. Hughes +4 more
doaj +1 more source
Gentamicin Pharmacokinetics in Term Neonates Receiving Extracorporeal Membrane Oxygenation [PDF]
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90148/1/j.1875-9114.1992.tb02667.x ...
Bhatt‐mehta, Varsha +2 more
core +1 more source
A 27-year-old primiparous woman with 28 weeks gestational age was admitted to our hospital with worsening shortness of breath. She was diagnosed with Ebstein’s anomaly three years ago, but preferred to be left untreated. The patient was not cyanotic and
Lusiani Rusdi +4 more
doaj +2 more sources

