Results 51 to 60 of about 6,089 (248)
Ventricular‐Vascular Coupling in Marfan and Non‐Marfan Aortopathies [PDF]
Background: Marfan syndrome (MFS) and familial non–syndromal thoracic aortic aneurysm and dissection (ns‐TAAD) are genetic aortopathies causing aortic dilatation with increased aortic stiffness.
Hambly, Brett +7 more
core +1 more source
Obstetric considerations for aortopathy in pregnancy
Aortic dissection (AD) associated with pregnancy can have catastrophic consequences for the mother and/or fetus. AD occurs in 4-5 per 1,000,000 pregnancies and, despite its rarity, is the third most frequent maternal cardiovascular cause of death. AD associated with pregnancy is most likely to occur in the third trimester or postpartum period.
Whelan, Anna R. +3 more
openaire +2 more sources
Abstract Purpose This study investigated the effect of bicuspid aortic valve (BAV) morphology and ascending aortic curvature (AAAc) bending angles on aortic hemodynamics, focusing on transvalvular jets and secondary helical flows that contribute to systolic hemodynamic stress linked to aortic complications.
Kaoru Hattori +6 more
wiley +1 more source
Cardiovascular genetic counselor decision making about discussing life insurance with patients
Abstract Genetic counselors (GCs) educate patients about the benefits, risks, and limitations of genetic testing. The regulatory environment governing the use of genetic data in life insurance is not uniform internationally or within the United States (US).
Sara Cherny +4 more
wiley +1 more source
Fibulin-4 is essential for maintaining arterial wall integrity in conduit but not muscular arteries [PDF]
Homozygous or compound heterozygous mutations in fibulin-4 (FBLN4) lead to autosomal recessive cutis laxa type 1B (ARCL1B), a multisystem disorder characterized by significant cardiovascular abnormalities, including abnormal elastin assembly, arterial ...
Broekelmann, Thomas J +5 more
core +3 more sources
A comprehensive model integrating clinical, imaging, and socioeconomic data improves prediction of disease progression and outcomes in moderate aortic stenosis, supporting a shift toward personalized assessment and management. ABSTRACT Background Despite increased awareness of its clinical consequences, personalized risk stratification in patients with
Alex D'Amico +7 more
wiley +1 more source
Bovine aortic arch with supravalvular aortic stenosis
A 5-year-old boy was diagnosed to have supravalvular aortic stenosis (SVAS). On evaluation of CT angiogram, there was associated bovine aortic arch (BAA).
Mohammed Idhrees +5 more
doaj +1 more source
The flowchart of the study. BAPN, β‐aminopropionitrile; FUMA, Functional Mapping and Annotation; GO, Gene Ontology; GWAS, genome‐wide association study; KEGG, Kyoto encyclopedia of genes and genomes; LDSC, LD score regression; MR‐JTI, mendelian randomization joint‐tissue imputation; MTAG, multi‐trait analysis of GWAS; siRNA, small interfering RNA ...
Qingyang Song +6 more
wiley +1 more source
Objective: We investigated the frequency of different bicuspid aortic valve disease (BAV) phenotypes,the associated valvular pathologies, and the aortopathy phenotypes, using 2-dimensional (2D) transthoracic, 2D transesophageal echocardiography (TEE) and
Selcen Yakar Tülüce +9 more
doaj +1 more source
Biomarkers of Aortopathy in Marfan Syndrome [PDF]
Marfan Syndrome (MFS) is an autosomal dominant, genetically inherited connective tissue disorder which primarily affects the cardiovascular system, but can also have systemic manifestations. First described in 1896, MFS has a prevalence of around 1/5000 in the general population. It is becoming increasingly common to see patients with MFS in a clinical
Iskandar, Zaid +4 more
openaire +3 more sources

