Results 11 to 20 of about 6,089 (248)
Aortopathy – A surgical pathology experience
Background: Aortopathy is a non-inflammatory and non-atherosclerotic disease of aorta that results from significant ‘degenerative’ changes in the media. This often leads to thoracic aortic aneurysms and/or dissections in young individuals.
Pradeep Vaideeswar, Sujit Udayaravi
doaj +3 more sources
Embryological Divergence and Molecular Mechanisms in Thoracic and Abdominal Aortic Aneurysms: Bridging Developmental Biology and Clinical Insights [PDF]
Aortic aneurysms are complex, predominantly asymptomatic vascular diseases with distinct incidence patterns depending on anatomical localisation. The incidence of thoracic aortic aneurysms (TAAs) has moderately increased, whereas that of abdominal aortic
Mathias Van Hemelrijck +5 more
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Background: Using echocardiographic surveillance, many patients are diagnosed with bicuspid aortic valve (BAV) without significant valve dysfunction. Limited data are available regarding the progression and outcomes of non-dysfunctional BAV.Methods and ...
Shinjeong Song +5 more
doaj +1 more source
Long-term outcomes in heritable thoracic aortic disease
Heritable aortic aneurysm is an increasingly recognized cause of morbidity and mortality. Whilst Marfan syndrome (MFS) is well-known, the clinical presentation and prognosis of more newly described genetic syndromes is less familiar to clinicians.
Elizabeth N. Robertson +7 more
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Clinical implications of the biomechanics of bicuspid aortic valve and bicuspid aortopathy
Bicuspid aortic valve (BAV), which affects up to 2% of the general population, results from the abnormal fusion of the cusps of the aortic valve. Patients with BAV are at a higher risk for developing aortic dilatation, a condition known as bicuspid ...
Ali Fatehi Hassanabad +9 more
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A Multidisciplinary Aortopathy Clinic: The McGill Experience. [PDF]
Kodaira M +12 more
europepmc +3 more sources
Background Primary and secondary aortopathy are frequently encountered in patients with congenital heart disease. The aim of this study is to present our experience and the incidence of primary and secondary adult CHD-associated aortopathy.
Ingrid Schusterova +4 more
doaj +1 more source
MiR-145 expression and rare NOTCH1 variants in bicuspid aortic valve-associated aortopathy. [PDF]
MicroRNAs (miRNAs) may serve as elegant tool to improve risk stratification in bicuspid aortic valve (BAV)-associated aortopathy. However, the exact pathogenetic pathway by which miRNAs impact aortopathy progression is unknown.
Evaldas Girdauskas +6 more
doaj +1 more source
PurposeCurrent intervention guidelines for bicuspid aortic valve (BAV) associated ascending aorta (AAo) dilatation are suboptimal predictors of clinical outcome.
Jiaxing Jason Qin +10 more
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TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome. [PDF]
Turner syndrome is caused by complete or partial loss of the second sex chromosome, occurring in ~1 in 2,000 female births. There is a greatly increased incidence of aortopathy of unknown etiology, including bicuspid aortic valve (BAV), thoracic aortic ...
Holly Corbitt +7 more
doaj +1 more source

