Results 281 to 290 of about 65,088 (328)

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

open access: yesCirculation Research, 2019
Rationale: Familial recurrence studies provide strong evidence for a genetic component to the predisposition to sporadic, nonsyndromic Tetralogy of Fallot (TOF), the most common cyanotic congenital heart disease phenotype. Rare genetic variants have been
Matthieu J Miossec   +2 more
exaly   +2 more sources

Tetralogy of Fallot and absent pulmonary valve syndrome.

Multimedia Manual of Cardio-Thoracic Surgery, 2022
Absent pulmonary valve syndrome is a relatively rare condition, representing a subset of about 3% of cases of tetralogy of Fallot in both autopsy and clinical reviews (1).
A. Virgone, H. Nuri
semanticscholar   +1 more source

Tetralogy of Fallot

Cardiology Clinics, 2020
Repaired tetralogy of Fallot is one of the most common conditions managed by adult congenital heart disease providers. Recent comprehensive review articles and book chapters are devoted to this topic. The purpose of this article is to address several common clinical questions encountered in the management of patients with repaired tetralogy of Fallot ...
Eric V, Krieger, Anne Marie, Valente
openaire   +4 more sources

Evaluation of Fetal Cardiac Size and Shape: A New Screening Tool to Identify Fetuses at Risk for Tetralogy of Fallot

Journal of ultrasound in medicine, 2021
Prenatal detection rates for tetralogy of Fallot (TOF) vary between 23 and 85.7%, in part because of the absence of significant structural abnormalities of the 4‐chamber view (4CV), as well as the relative difficulty in detection of abnormalities during ...
G. Devore   +4 more
semanticscholar   +1 more source

Prediction of prognosis in patients with tetralogy of Fallot based on deep learning imaging analysis

Heart, 2020
Objective To assess the utility of machine learning algorithms for automatically estimating prognosis in patients with repaired tetralogy of Fallot (ToF) using cardiac magnetic resonance (CMR).
G. Diller   +8 more
semanticscholar   +1 more source

Tetralogy of Fallot

Multimedia Manual of Cardio-Thoracic Surgery, 2006
The optimal management of patients with tetralogy of Fallot has to consider the individual intra-cardiac anatomy as the most important variable, together with the age and the body weight of the patient. In any case the potential advantages of a primary early repair should be weighted against the experience and expertise of the individual centre and/or ...
Pozzi, M., Quarti, A., Corno, A. F.
openaire   +3 more sources

Tetralogy of Fallot

Seminars in Thoracic and Cardiovascular Surgery, 2015
Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease beyond 1 week of age. “Classic” TOF usually presents for surgical repair during the first 3–9 months of life. Surgical repair techniques vary among surgeons and institutions. The optimal timing and approach to complete (vs. staged) surgical repair remain a topic of continued
Charles D, Fraser   +5 more
openaire   +4 more sources

Tetralogy of fallot

Current Treatment Options in Cardiovascular Medicine, 2001
The optimal surgical approach and timing for patients with tetralogy of Fallot remain controversial. There are two options in current practice: a two-stage repair (an initial palliative aortopulmonary shunt at an early age followed by complete repair at an older age) or primary complete repair.
Gouw, Samantha C.   +2 more
openaire   +3 more sources

Tetralogy of Fallot

Pediatric Clinics of North America, 1990
Tetralogy of Fallot is the most common malformation of children born with cyanotic heart disease, with an incidence of approximately 10 per cent of congenital heart disease. There can be a wide spectrum as to the severity of the anatomic defects, which include ventricular septal defect, aortic override, right ventricular outflow tract obstruction, and ...
Pinsky, WW, Arciniegas, E
openaire   +2 more sources

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