Results 31 to 40 of about 3,161 (171)

Ebstein’s Anomaly, Left Ventricular Noncompaction, and Sudden Cardiac Death

open access: yesCase Reports in Cardiology, 2015
Ebstein’s anomaly is a congenital disorder characterized by apical displacement of the septal leaflet of the tricuspid valve. Ebstein’s anomaly may be seen in association with other cardiac conditions, including patent foramen ovale, atrial septal ...
Michael McGee   +2 more
doaj   +1 more source

Functional Critical Aortic Stenosis with Transient Retrograde Flow in a Neonate with Left Diaphragmatic Hernia [PDF]

open access: yes, 2012
We report a neonate with left congenital diaphragmatic hernia and severe left ventricular dysfunction, in whom the blood flow in the transverse arch and its branches was supported in a retrograde fashion by patent ductus arteriosus.
Aggarwal, Sanjeev   +2 more
core   +1 more source

Prenatal detection and outcome of major heart defects in a country with universal screening

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective To evaluate the Danish prenatal screening program for major fetal congenital heart defects (mCHD), focusing on incidence, detection rates (DRs), pregnancy outcomes and postnatal mortality. Methods This was a 5‐year nationwide cohort study conducted from January 2018 to December 2022 in Denmark.
C. Vedel   +15 more
wiley   +1 more source

Tricuspid valve dysplasia in dogs [PDF]

open access: yes, 2018
A general overview of tricuspid valve dysplasia in dogs is presented in this review. This congenital disease has been described in numerous large dog breeds but especially the Labrador retriever is predisposed.
Bavegems, Valérie   +5 more
core   +1 more source

Cardiovascular Health in Women—Across the Lifespan

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar   +5 more
wiley   +1 more source

Management and outcome of Ebstein's anomaly in children [PDF]

open access: yes, 2017
Objectives To assess clinical presentation, treatment, and outcome of children with Ebstein's anomaly. Background Data on long-term outcome of children with Ebstein's anomaly are scarce.
Attenhofer Jost, Christine H.   +8 more
core  

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network

open access: yesPaediatric and Perinatal Epidemiology, EarlyView.
ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman   +23 more
wiley   +1 more source

Ebstein Anomaly in Pregnancy

open access: yesActa Medica Indonesiana, 2017
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

Supraventricular Tachycardias Using Multiple Accessory Pathways

open access: yesJournal of Arrhythmia, Volume 42, Issue 1, February 2026.
Three atrioventricular reciprocating tachycardias (AVRTs) using 3 accessory pathways (APs) occurred with the His bundle eliminated by the previous ablation. Two AVRTs using 2 right APs rotated reversely, and the other AVRT was one with a retrograde conduction through the left AP and anterograde conduction through the 2 right APs.
Takumi Yamada
wiley   +1 more source

Ultrassonografia tridimensional STIC-HDlive no modo de superfície: nova técnica para avaliação do coração fetal [PDF]

open access: yes, 2013
Universidade Federal de São Paulo (UNIFESP) Department of ObstetricsUNIFESP, Department of ...
Araujo Júnior, Edward   +2 more
core   +2 more sources

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