Results 11 to 20 of about 42,317 (250)

Congenital Heart Disease In Preterm Infants

Diyala Journal of Medicine, 2023
Background: Congenital heart defects and preterm birth  are two important causes of neonatal and infant mortality. However, the relationship between them has not yet been fully clarified. Objective: To find the association of congenital heart disease
Maymouna A Jassam ,, Najdat S. Mahmood ,, Sura Q. Mahmood   +2 more
doaj   +1 more source

Altered Cerebral Microstructure in Adults With Atrial Septal Defect and Ventricular Septal Defect Repaired in Childhood

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2022
Background Delayed brain development, brain injury, and neurodevelopmental disabilities are commonly observed in infants operated for complex congenital heart defect. Our previous findings of poorer neurodevelopmental outcomes in individuals operated for
Benjamin Asschenfeldt, Lars Evald, Camilla Salvig, Johan Heiberg, Leif Østergaard, Simon Fristed Eskildsen, Vibeke Elisabeth Hjortdal   +6 more
doaj   +1 more source

O-linked β-N-acetylglucosamine transferase plays an essential role in heart development through regulating angiopoietin-1.

PLoS Genetics, 2020
O-linked N-acetylglucosamine (GlcNAc) transferase (OGT) is the only enzyme catalyzing O-GlcNAcylation. Although it has been shown that OGT plays an essential role in maintaining postnatal heart function, its role in heart development remains unknown ...
Yongxin Mu, Houzhi Yu, Tongbin Wu, Jianlin Zhang, Sylvia M Evans, Ju Chen   +5 more
doaj   +1 more source

Coxsackievirus B3 Infection Early in Pregnancy Induces Congenital Heart Defects Through Suppression of Fetal Cardiomyocyte Proliferation

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021
Background Coxsackievirus B (CVB) is the most common cause of viral myocarditis. It targets cardiomyocytes through coxsackie and adenovirus receptor, which is highly expressed in the fetal heart.
Vipul Sharma, Lisa S. Goessling, Anoop K. Brar, Chetanchandra S. Joshi, Indira U. Mysorekar, Pirooz Eghtesady   +5 more
doaj   +1 more source

Holt-Oram Syndrome in Adult Presenting with Heart Failure: A Rare Presentation

Case Reports in Cardiology, 2014
Holt-Oram syndrome is a rare inherited disorder involving the hands, arms, and the heart. The defects involve carpal bones of the wrist and the thumb and the associated cardiac anomalies like atrial or ventricular septal defects.
Rupesh Kumar, Subhendu Sekhar Mahapatra, Monalisa Datta, Amanul Hoque, Swarnendu Datta, Soumyajit Ghosh, Santanu Datta, Subhankar Bhattacharjee   +7 more
doaj   +1 more source

Atrial septal defect with a rare occupying lesion in heart

BMC Cardiovascular Disorders, 2022
Abstract Background Cardiac epicardium hemangiomas are exceedingly rare; however, they can cause significant hemodynamic impairment and large pericardial effusions. On rare occasion, cardiac tumors coexist with malformations of the heart.
Jinlan Chen, Xueyang Gong, Li Xie, Qin Wu, Tianli Zhao, Shijun Hu   +5 more
openaire   +3 more sources

Incidence and Types of Congenital Heart Diseases among Children in Sulaimani Governorate

Kurdistan Journal of Applied Research, 2017
Congenital heart diseases (CHD) are common causes of cardiovascular morbidity and mortality among young children and adolescents. It is the most common form of structural congenital defects.
Niaz Kamal, Nasih Othman, Aso Salih
doaj   +1 more source

Genetic Insights into Congenital Cardiac Septal Defects—A Narrative Review

Biology
Congenital heart diseases (CHDs) are a group of complex diseases characterized by structural and functional malformations during development in the human heart; they represent an important problem for public health worldwide.
Jorge L. Cervantes-Salazar, Nonanzit Pérez-Hernández, Juan Calderón-Colmenero, José Manuel Rodríguez-Pérez, María G. González-Pacheco, Clara Villamil-Castañeda, Angel A. Rosas-Tlaque, Diego B. Ortega-Zhindón   +7 more
doaj   +1 more source

Simultaneous transcatheter closure of intralobar pulmonary sequestration and patent ductus arteriosus in a patient with infantile Scimitar syndrome

Türk Kardiyoloji Derneği Arşivi, 2015
Scimitar syndrome is a rare disease associated with a right lung sequestration vascularised by arteries arising from the abdominal aorta and abnormal venous drainage into the inferior vena cava. The infantile form is generally presented with severe heart
Eyup Aslan, Ibrahim Cansaran Tanidir, Murat Saygi, Sertac Hanedan Onan, Alper Guzeltas   +4 more
doaj   +1 more source

Epigenetic Evaluation of the TBX20 Gene and Environmental Risk Factors in Mexican Paediatric Patients with Congenital Septal Defects

Cells, 2023
The TBX20 gene has a key role during cardiogenesis, and it has been related to epigenetic mechanisms in congenital heart disease (CHD). The purpose of this study was to assess the association between DNA methylation status and congenital septal defects ...
Esbeidy García-Flores, Juan Calderón-Colmenero, Verónica Marusa Borgonio-Cuadra, Juan Pablo Sandoval, José Antonio García-Montes, Benny Giovanni Cazarín-Santos, Antonio Miranda-Duarte, Armando Gamboa-Domínguez, José Manuel Rodríguez-Pérez, Nonanzit Pérez-Hernández   +9 more
doaj   +1 more source