Results 31 to 40 of about 121,138 (267)
Commentary: Double-outlet right ventricle revisited [PDF]
The Journal of Thoracic and Cardiovascular Surgery, 2019 Carl L. Backer
openalex +3 more sources
Co-occurrence of Carpenter syndrome and double outlet right ventricle
Türk Kardiyoloji Derneği Arşivi, 2017 Carpenter syndrome (Acrocephalopolysyndactyly type 2, OMIM 201000) is a rarely seen autosomal recessive disorder. In addition to abnormalities such as acrocephaly, craniosynostosis, facial asymmetry, polydactyly and syndactyly, obesity, hypogonadism ...
Osman Güvenç +3 more
doaj +1 more source
Ultrasound in Obstetrics and Gynecology, 2020 To analyze the incremental benefit of 3D/4D spatiotemporal image correlation (STIC) fetal echocardiography over 2D fetal echocardiography with respect to the accuracy of identification of anatomic details crucial for surgical decision‐making and in ...
B. Karmegaraj +5 more
semanticscholar +1 more source
Isolated double chambered right ventricle as a rare cause of sudden death in infancy
Egyptian Journal of Forensic Sciences, 2016 Isolated double-chambered right ventricle (DCRV) is a rare form of congenital heart disorder in which the right ventricle is divided into a high-pressure inlet portion and a low-pressure outlet portion by an anomalous muscle bundle. Rarely, autopsy cases
W. Thaljawi +8 more
doaj +1 more source
Double-outlet right ventricle revisited [PDF]
The Journal of Thoracic and Cardiovascular Surgery, 2017 Double-outlet right ventricle is a form of ventriculoarterial connection. The definition formulated by the International Society for Nomenclature of Paediatric and Congenital Heart Disease is based on hearts with both arterial trunks supported in their greater part by a morphologically right ventricle.
University of Florida Health Congenital Heart Center, Gainesville, Fla ( host institution ) +5 more
openaire +4 more sources
Russian Open Medical Journal, 2015 Congenital heart disease is a major cause of morbidity and mortality. Single ventricle is a rare finding and usually of left ventricular morphology. We present here interesting antenatal and postnatal echocardiographic findings of a baby having a rare ...
Donboklang Lynser, Evarisalin Marbaniang
doaj +1 more source
A computational study of aortic reconstruction in single ventricle patients [PDF]
arXiv, 2022 Patients with hypoplastic left heart syndrome (HLHS) are born with an underdeveloped left heart. They typically receive a sequence of surgeries that result in a single ventricle physiology called the Fontan circulation. While these patients usually survive into early adulthood, they are at risk for medical complications, partially due to their lower ...
arxiv
Double outlet right ventricle with mitral atresia in an adult with minimal symptoms
IHJ Cardiovascular Case Reports, 2021 A 35-year old man sustained fracture of cervical vertebrae in an automobile accident and pre-operative routine echocardiography showed double outlet right ventricle (DORV) with infundibular and valvar pulmonary stenosis, mitral atresia, hypoplastic left ...
Madhu Shukla, Jagdish C. Mohan
doaj
Semi-Supervised Segmentation of Multi-vendor and Multi-center Cardiac MRI using Histogram Matching [PDF]
IEEE Conference on Signal Processing and Communications
applications (SIU 2021), 2023 Automatic segmentation of the heart cavity is an essential task for the diagnosis of cardiac diseases. In this paper, we propose a semi-supervised segmentation setup for leveraging unlabeled data to segment Left-ventricle, Right-ventricle, and Myocardium. We utilize an enhanced version of residual U-Net architecture on a large-scale cardiac MRI dataset.
arxiv
Epigastric heteropagus associated with an omphalocele and double outlet right ventricle
Journal of Pediatric Surgery Case Reports, 2015 Incomplete or asymmetrical conjoined twins are extremely rare congenital anomalies. We report a case of epigastric heteropagus associated with an omphalocele and double outlet right ventricle.
Tatsuma Sakaguchi +5 more
doaj +1 more source