Results 51 to 60 of about 55,310 (326)

Pulmonary Valve Replacement for Tetralogy of Fallot.

Methodist DeBakey Cardiovascular Journal, 2019
Right ventricular outflow tract (RVOT) dysfunction is common following surgical repair of tetralogy of Fallot and other forms of complex congenital heart disease.
D. Balzer
semanticscholar   +1 more source

Tetralogy of Fallot Associated with Right Arch and Persistent Left Dorsal Aortic Aneurysm

, 2012
We described a patient who was diagnosed of Tetralogy of Fallot with right arch. Dorsal aortic aneurysm was found later confirmed by cardiac catheterization and reconstruction of 3D computer tomography.
Chang, Hok-Keong; Wang, Jieh-Neng; Hung, Wen-Pin; Chen, Shyn-Jye; Wu, Jing-Ming, 王玠能;陳世杰;吳俊明   +1 more
core   +1 more source

Usage of 3D models of tetralogy of Fallot for medical education: impact on learning congenital heart disease

BMC Medical Education, 2017
BackgroundCongenital heart disease (CHD) is the most common human birth defect, and clinicians need to understand the anatomy to effectively care for patients with CHD.
Y. Loke, Ashraf S. Harahsheh, Axel Krieger, L. Olivieri   +3 more
semanticscholar   +1 more source

Oral and systemic manifestations, and dental management of a pediatric patient with Tetralogy of Fallot. A case report.

Journal of Oral Research, 2016
Introduction: Tetralogy of Fallot is a congenital heart disease and the most common cyanotic heart defect in children. It is clinically characterized by a ventricular septal defect, pulmonary stenosis, overriding aorta over ventricular septal defect and ...
Carmen Ayala, Lizbeth Aguayo
doaj   +1 more source

Congenital absence of sternum with tetralogy of Fallot, right aortic arch, and bilateral superior vena cava

Egyptian Pediatric Association Gazette, 2023
Background Congenital complete absence of sternal bone or cleft sternum or absent sternum is a very rare and potentially life-threatening birth defect.
Santosh Chavan, Nilima Narkhede, Rajaram Weling   +2 more
doaj   +1 more source

Dysphagia in an adult tetralogy of fallot with double aortic arch [PDF]

, 2013
Double aortic arch (DAA) is a common vascular ring. It may occur in isolation or coexist with various types of congenital heart disease . The anomaly usually presents in early infancy.
Bhan, Anil, Munesh, Tomar, Pankaj, Bhatiya   +2 more
core  

De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype–Phenotype Correlation and Development of a CGR Detection Pipeline

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle, Jesse D. Bengtsson, Mira Gandhi, Christopher M. Grochowski, Ming Yin Lun, Neha Sudhir, Shalini N. Jhangiani, Fritz J. Sedlazeck, Seema R. Lalani, Neil A. Hanchard, Claudia M. B. Carvalho   +10 more
wiley   +1 more source

Outcome of humanitarian patients with late complete repair of tetralogy of Fallot: A 13-year long single-center experience

International Journal of Cardiology Congenital Heart Disease, 2022
Background: Surgical repair of tetralogy of Fallot is usually performed between 3 and 6 months of age with pulmonary valve-sparing repair promoted for the best long-term result.
Damien Schaffner, Guillaume Maitre, Sebastiano A.G. Lava, Yann Boegli, Mirko Dolci, Raymond Pfister, Nicole Sekarski, Perez Marie-Hélène, Stefano Di Bernardo   +8 more
doaj   +1 more source

Management of Tetralogy of Fallot with Pulmonary Atresia [PDF]

, 2005
Tetralogy of Fallot with Pulmonary Atresia is an extreme form of tetralogy characterized by absence of flow from the right ventricle to the pulmonary arteries.
Prieto, Lourdes R.
core  

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source