Results 71 to 80 of about 48,714 (242)
Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers
Background Impaired myocardial blood flow (MBF) in the absence of epicardial coronary disease is a feature of hypertrophic cardiomyopathy (HCM). Although most evident in hypertrophied or scarred segments, reduced MBF can occur in apparently normal segments.
Rebecca K. Hughes +14 more
wiley +1 more source
Feasibility of Imaging the Uvula at the Midtrimester Anomaly Ultrasound
Objectives The fetal palate is not routinely imaged as part of the midtrimester fetal anomaly ultrasound, despite being associated with many syndromes. The “equal sign” depicts the lateral borders of the uvula on 2‐dimensional fetal ultrasound. We assessed the feasibility of adding the equal sign to the midtrimester fetal anomaly ultrasound.
Anna Rose Sims +3 more
wiley +1 more source
Sudden Death of a 17‐Month‐Old Chimpanzee (Pan troglodytes) due to a Congenital Undiagnosed Ventricular Septal Defect [PDF]
ABSTRACT Ventricular septal defect (VSD) is a congenital defect that is frequently observed in humans. We report the sudden death of an infant chimpanzee due to a congenital undiagnosed VSD. During necropsy, the examination of the heart revealed a VSD, dilatation of the left ventricle and myocardial hypertrophy of the right ventricle.
Kondova I +3 more
europepmc +2 more sources
ABSTRACT Diabetic cardiomyopathy (DCM) is a common complication of diabetes mellitus. This study investigated the effects of alogliptin on DCM and its underlying mechanisms. A DCM model was constructed and treated with alogliptin. Downstream targets of alogliptin were screened using bioinformatics analysis.
Li‐Jing Jiao +7 more
wiley +1 more source
PENTALOGÍA DE FALLOT. PRESENTACIÓN DE UN PACIENTE / Fallot’s Pentalogy. Presentation of a patient [PDF]
In 1888, Etienne Fallot described the last two components of Fallot’s tetralogy: right ventricular hypertrophy and dextroposition of the aorta over septal defect.
Ana Miriam Clemades Méndez +2 more
doaj
Longest survivor of pulmonary atresia with ventricular septal defect without surgical intervention
ESC Heart Failure, Volume 12, Issue 2, Page 1499-1507, April 2025.
Sang Zhou +5 more
wiley +1 more source
Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation
We report the first documented case of airway involvement in Conradi–Hünermann–Happle syndrome (CDPX2), an X‐linked dominant form of chondrodysplasia punctata caused by pathogenic variants in EBP. A 2‐month‐old female with genetically confirmed CDPX2 developed severe subglottic stenosis and persistent respiratory distress requiring CPAP; cross ...
Enrique G. Villarreal +3 more
wiley +1 more source
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa +7 more
wiley +1 more source
Diagnostic Yield of Post‐Mortem Fetal Micro‐CT for Thoracic Abnormalities
ABSTRACT Objective This study aims to identify the imaging findings specifically for thoracic anomalies in 1200 Micro‐CT cases, independent of whether the abnormality contributed to the main diagnosis or cause of death. Method We analyzed 1200 Micro‐CT scans in an unselected, consecutive cohort between 2017 and 2024 to identify thoracic anomalies ...
Ian C. Simcock +5 more
wiley +1 more source
Background. B-type natriuretic peptide has been shown to be a very sensitive and specific marker of heart failure. In this study, we aimed to investigate the effect of percutaneous closure of ventricular septal defects with Amplatzer septal occluders on ...
Yuksel Kaya +11 more
doaj +1 more source

