Results 21 to 30 of about 93,808 (313)

Genetic Diagnostics Contribute to the Risk Stratification for Major Arrhythmic Events in Pediatric Patients with Long QT Syndrome Type 1–3

Cardiogenetics, 2022
Long QT syndrome (LQTS) is an inherited arrhythmic disorder associated with sudden cardiac death (SCD). This study aimed to identify the clinical and molecular genetic risk factors that contribute to major arrhythmic events (MAEs) in patients with ...
Tobias Burkard, Dominik Sebastian Westphal, Franziska Markel, Roman Antonin Gebauer, Gabriele Hessling, Cordula Maria Wolf   +5 more
doaj   +1 more source

New Insights into the Education of Children with Congenital Heart Disease with and without Trisomy 21

Medicina, 2023
Background and Objectives: Patients with congenital heart disease (CHD), especially as a concomitant syndromal disease of trisomy 21 (T21), are at risk for impaired neurodevelopment. This can also affect these patients’ education.
Katharina R. L. Schmitt, Laura K. Sievers, Alina Hütter, Hashim Abdul-Khaliq, Martin Poryo, Felix Berger, Ulrike M. M. Bauer, Paul C. Helm, Constanze Pfitzer   +8 more
doaj   +1 more source

Polymalformative syndrome with congenital heart defect [PDF]

Einstein (São Paulo), 2015
Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Lisboa, Portugal.Corresponding author: Sara Pimentel Marcos – Hospital de Sao Francisco Xavier, Estrada do Forte do Alto do Duque − Sao Francisco Xavier − Zip code: 1449-005 − Lisboa, Portugal − Phone: +00351210431441 E-mail: sarasenamarcos@gmail.comReceived on: Aug 5, 2013 – Accepted on: Mar ...
Sara Pimentel Marcos, Anabela Salazar, Teresa Castro, Rui Anjos   +3 more
openaire   +4 more sources

Assessment of anatomy of the aorta in patients with a coarctation of aorta

The Cardiothoracic Surgeon, 2023
Background Coarctation of the aorta (CoA) is a congenital heart disease characterized by the narrowing of the aorta, resulting in reduced blood flow to the body and increased pressure in the left ventricle.
B. B. Turaev, Kh. K. Abralov, B. Kh. Kobiljonov, N. Sh. Ibragimov   +3 more
doaj   +1 more source

CONGENITAL HEART DEFECTS

, 2023
Congenital heart defects (TYN), also known as congenital heart anomaly and congenital heart disease, are defects in the structure of the heart or great vessels present at birth. Congenital heart defects are classified as cardiovascular diseases. Signs and symptoms depend on the specific type of defect. Symptoms can be harmless or life-threatening.
openaire   +1 more source

Nationwide Survey Reveals High Prevalence of Non-Swimmers among Children with Congenital Heart Defects

Children, 2023
Background: Physical activity is important for children with congenital heart defects (CHD), not only for somatic health, but also for neurologic, emotional, and psychosocial development. Swimming is a popular endurance sport which is in general suitable
Christian Apitz, Dominik Tobias, Paul Helm, Ulrike M. Bauer, Claudia Niessner, Jannos Siaplaouras   +5 more
doaj   +1 more source

Spatio-Temporal Distribution and Demographic Characteristics of Congenital Heart Defects in Guangdong, China, 2016–2020

Frontiers in Public Health, 2022
BackgroundCongenital heart defects are the most common type of birth defects and bring a heavy disease burden in China. Examining the temporal and spatial trends of congenital heart defects epidemics can give some elementary knowledge for succeeding ...
Huazhang Miao, Huazhang Miao, Huazhang Miao, Qinghui Zeng, Zengping Shi, Yi Xia, Lushaobo Shi, Dongxue Chen, Pi Guo, Yingxian Zhu, Dong Wang   +10 more
doaj   +1 more source

Interventional Partial Cavopulmonary Connection: Initial Clinical Experience With Acute Procedural up to Midterm Results

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Creation of a partial cavopulmonary anasthomosis in patients with isolated right‐sided heart failure or patients with cyanosis and intracardial right‐to‐left shunt and reduced blood flow in the pulmonary circulation may provide a significant ...
Katarzyna Gendera, Peter Ewert, Stanimir Georgiev, Andreas Eicken, Daniel Tanase, Kristina Borgmann, Paul Philipp Heinisch, Nicole Nagdyman, Julie Cleuziou, Dunja Renner, Pinar Bambul Heck   +10 more
doaj   +1 more source

It Is Not Carved in Stone—The Need for a Genetic Reevaluation of Variants in Pediatric Cardiomyopathies

Journal of Cardiovascular Development and Disease, 2022
(1) Background: In cardiomyopathies, identification of genetic variants is important for the correct diagnosis and impacts family cascade screening. A classification system was published by the American College of Medical Genetics and Genomics (ACMG) in ...
Dominik Sebastian Westphal, Kathrin Pollmann, Christoph Marschall, Annette Wacker-Gussmann, Renate Oberhoffer-Fritz, Karl-Ludwig Laugwitz, Peter Ewert, Cordula Maria Wolf   +7 more
doaj   +1 more source

Spectrum of congenital heart defects in Croatia

European Journal of Pediatrics, 2009
The aim of our study was to investigate the incidence of congenital defects in children born in Croatia during a period of 5 years, its association with extracardiac malformations, its treatment, and outcome. Medical information about the patients was obtained from 14 paediatric cardiology centres that cover the whole country.
Dilber, Daniel, Malčić, Ivan
openaire   +5 more sources