Results 11 to 20 of about 27,131 (277)

Cardiovascular Abnormalities Associated with Heterotaxy Syndrome: A Case Series

open access: yesJournal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2023
Heterotaxy syndromes result from the failure of normal lateralization, resulting in the abnormal arrangement of cardiothoracic and abdominal viscera. These are associated with a disproportionate morbidity and mortality rate, mandating early diagnosis ...
Shraddha Joshi   +3 more
doaj   +1 more source

Thoracic Aorta: Anatomy and Pathology

open access: yesDiagnostics, 2023
The aorta is the largest elastic artery in the human body and is classically divided into two anatomical segments, the thoracic and the abdominal aorta, separated by the diaphragm.
Cira Rosaria Tiziana di Gioia   +3 more
doaj   +1 more source

Fetal heterotaxy with tricuspid atresia, pulmonary atresia, and isomerism of the right atrial appendages at 22 weeks. [PDF]

open access: yes, 2013
We report the accurate prenatal diagnosis at 22 weeks gestation of right atrial isomerism in association with tricuspid atresia. Several distinctive sonographic features of isomerism of the right atrial appendages were present in this fetus: complex ...
Richardson, Randy R   +3 more
core   +2 more sources

Partial upper sternotomy for extensive arch repair in older acute type A aortic dissection patients

open access: yesBMC Cardiovascular Disorders, 2022
Objectives The partial upper sternotomy (PUS) approach is acceptable for aortic valve replacement, and even aortic root operation. However, the efficiency of PUS for extensive arch repair of acute type A aortic dissection (AAAD) in older adult patients ...
Zhihuang Qiu   +6 more
doaj   +1 more source

Left main bronchus compression due to main pulmonary artery dilatation in pulmonary hypertension: two case reports [PDF]

open access: yes, 2015
. Pulmonary arterial dilatation associated with pulmonary hypertension may result in significant compression of local structures. Left main coronary artery and left recurrent laryngeal nerve compression have been described.
Ariff, B   +6 more
core   +1 more source

Experience of diagnosis of congenital arterial anomaly in a child with bronchial obstruction: clinical case and summary

open access: yesZdorovʹe Rebenka, 2017
Congenital anomalies of the aortic arch are a large group of cardiovascular anomalies. Some of them are isolated; others are associated with congenital heart defects or genetic syndromes. There can be different clinical manifestations of these anomalies —
L.V. Besh   +8 more
doaj   +1 more source

Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog [PDF]

open access: yes, 2019
The atrioventricular canal defect (AVCD) is a congenital heart defect (CHD) frequently associated with extracardiac anomalies (75%). Previous observations from a personal series of patients with AVCD and "polydactyly syndromes" showed that the distinct ...
Baban, A   +9 more
core   +1 more source

Evaluation of Aortic Arch Disorders in Patients with Tetralogy of Fallot

open access: yesArmaghane Danesh Bimonthly Journal, 2021
Background & aim: Fallot tetralogy (TOF) is one of the most common diseases among congenital heart cyanotic abnormalities. 25% of these patients have a right aortic arch.
N Mehdizadegan   +3 more
doaj  

Impact of Geographic Location on Diagnosis and Initial Management of Takayasu Arteritis: A Tale of Two Cohorts from Italy and India

open access: yesDiagnostics, 2022
The present study compares disease characteristics, imaging modalities used, and patterns of treatment in two large cohorts of Takayasu arteritis (TAK) from Italy and India. Clinic files were retrospectively reviewed to retrieve information about initial
Durga Prasanna Misra   +14 more
doaj   +1 more source

Short-term and long-term outcomes in 133 429 emergency patients admitted with angina or myocardial infarction in Scotland, 1990-2000: population-based cohort study [PDF]

open access: yes, 2006
Objective: To analyse short- and long-term outcomes and prognostic factors in a large population-based cohort of unselected patients with a first emergency admission for suspected acute coronary syndrome between 1990 and 2000 in Scotland. Methods: All
Boyd, J.   +9 more
core   +2 more sources

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