Results 111 to 120 of about 55,310 (326)
Biallelic SLC20A1 loss‐of‐function variant causes a previously unrecognized multisystem developmental disorder. We report the first homozygous case presenting with tetralogy of Fallot, renal agenesis, polydactyly, and growth impairment. Transcriptome analysis of patient‐derived fibroblasts suggests significant dysregulation of pathways critical for ...
Eugénie Koumakis +9 more
wiley +1 more source
Arrhythmias After Tetralogy of Fallot Repair
Tetralogy of Fallot is the most common cyanotic congenital heart disease, with a good outcome after total surgical correction. In spite of a low perioperative mortality and a good quality of life, late sudden death remains a significant clinical problem,
Antonio Franco Folino +3 more
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Terson Syndrome in A Patient with Unrepaired Tetralogy of Fallot
Tetralogy of Fallot is the most commonly seen cyanotic congenital heart disease. It includes four cardinal features: right ventricular outflow tract obstruction, misaligned ventricular septal defect, overriding aorta, and concentric right ventricular ...
Ayaz, Ifrah +7 more
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ABSTRACT Introduction This study systematically synthesized evidence on adverse health outcomes related to gestational diabetes mellitus (GDM) via an umbrella review with integrated meta‐analyses. Methods The search covered publications from the database (PubMed/MEDLINE, Google Scholar, Embase, and CINAHL) inception to August 12, 2024. Meta‐analyses of
Jiseung Kang +14 more
wiley +1 more source
Aortic aneurysm formation five decades after tetralogy of Fallot repair.
Surgical repair of tetralogy of Fallot is recognized as one of the most successful palliative cardiac surgical procedures. We report a patient in whom cystic medial necrosis developed 50 years after tetralogy of Fallot repair that caused a pathologic ...
Wilson, Dirk +4 more
core +1 more source
ELABELA Targets Mitochondria to Modulate Heart Development
The role of peptide ELABELA (ELA) in cardiomyocyte apoptosis and congenital heart disease (CHD) is unclear. ELA deficiency caused cardiomyocyte apoptosis and CHD. A novel ELA‐APJ‐AKT‐BCL2/BAX axis in regulating mitochondrial function and contributing to CHD pathogenesis was established.
Jian Wang +22 more
wiley +1 more source
Thrombocytopenia absent radius syndrome with Tetralogy of Fallot: a rare association
Chetan Kumar,1 Deepak Sharma,2 Aakash Pandita,2 Sanjay Bhalerao1 1Department of Pediatrics, Madras Institute of Orthopedic and Trauma, Manapakkam, Chennai, India; 2Department of Neonatology, Fernandez Hospital, Hyderabad, India Abstract ...
Bhalerao S, Pandita A, Sharma D, Kumar C
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Health Care Utilization in Adults With Congenital Heart Disease: Population‐Based Findings
ABSTRACT Background Population‐based data on healthcare utilization in adults with congenital heart disease (CHD) are limited. We examined utilization patterns in a multi‐site, population‐based U.S. cohort of adults with CHD. Methods This retrospective cohort linked health and administrative records from five regions (Colorado, North Carolina, Utah ...
Tessa L. Crume +17 more
wiley +1 more source
BackgroundTetralogy of Fallot is one of the critical congenital heart defects needing intervention within the first year of life.ObjectiveThis review aims to systematically assess the prevalence of Tetralogy of Fallot among children and adolescents with ...
Biniam Endale Geleta, Abay Mulu
doaj +1 more source
Reoperation after radical correction tetralogy of Fallot: results and prospects
The aim – to present experience, results and prospects of repeated interventions in the remote period after radical correction of tetralogy of Fallot. Materials and methods. Results of the repeated 65 surgeries in 62 patients after radical correction of
L.R. Naumova +8 more
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