Results 31 to 40 of about 3,775 (165)
Long QT Syndrome Type 5 With Coexisting KCNE1 and RYR2 Variants: A Diagnostic Ambiguity
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Long QT syndrome (LQTS) predisposes to syncope and sudden cardiac death. Type 5 LQTS, linked to KCNE1 variants, is rare. A teenage female presented with recurrent syncope. ECG showed QTc 485 ms. Genetic testing identified KCNE1 and RYR2 variants. Beta‐blockers and ICD prevented events.
Mohammad Hossein Nikoo +4 more
wiley +1 more source
ATIPICIDADES EN UN CASO CON DISPLASIA ARRITMOGÉNICA DEL VENTRÍCULO DERECHO O ENFERMEDAD DE UHL / Report of an atypical case with arrhythmogenic right ventricular dysplasia or Uhl´s anomaly [PDF]
CorSalud, 2012 ResumenLa displasia arritmogénica del ventrículo derecho es una miocardiopatía caracterizada por arritmias ventriculares malignas y anomalías estructurales progresivas, que afectan primariamente al ventrículo derecho.
Aníbal González Trujillo +4 more
doaj
Cardiovascular Health in Women—Across the Lifespan
Clinical Endocrinology, Volume 104, Issue 6, Page 539-555, June 2026.ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar +5 more
wiley +1 more source
Alternative Lead ECG Placements
Annals of Noninvasive Electrocardiology, Volume 31, Issue 3, May 2026.Alternative ECG lead placements can improve diagnostic yield when the standard 12‐lead ECG is suboptimal or infeasible. This review summarizes practical, scenario‐driven modifications (right‐sided, posterior, seated/prone, Lewis, Fontaine, torso‐based, and monitoring configurations) to better detect ischemia, right ventricular disease/ARVD, and ...
José Luis Morales‐Arteaga +12 more
wiley +1 more source
Clinical Cardiology, Volume 49, Issue 4, April 2026.Methods and cohort: HF patients with normal to mild renal insufficiency (n = 637), divided into HFpEF, HFmrEF, and HFrEF. Statistical Method: Cox regression models, Kaplan‐Meier Curves, C‐index, IDI, and NRI. Findings: Over a follow‐up of 9.4 years, significant associations of elevated CysC levels with increased risks of all‐cause mortality and HF ...
Lyu Lyu +5 more
wiley +1 more source
Veterinary Record Case Reports, Volume 14, Issue 1, February 2026.Abstract A 10‐year‐old, female, spayed Pitbull mix presented for evaluation of an arrhythmia. Echocardiography revealed enlargement of all cardiac chambers and decreased left ventricular systolic function. Electrocardiography demonstrated isolated, ventricular premature complexes.
Nathan Mitchell +3 more
wiley +1 more source
Arrhythmogenic Right Ventricular Dysplasia — a Variant of Primary Cardiomyopathy
Zdorovʹe Rebenka, 2013 This article provides an own observation of family form of arrhytmogenic right ventricular dysplasia in a girl, which had been followed-up for 12 years.
G.E. Sukhareva, V.I. Sadovoy
doaj +1 more source
Chinese Clinical Practice Guidelines for Auditory Neuropathy (gCAN)
World Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 12, Issue 1, Page 1-24, February 2026.ABSTRACT Auditory neuropathy (AN) is an auditory disorder that affects the function of the auditory pathway. An increasing number of AN cases have been identified with the revelation of the underlying mechanisms, the advancements of diagnostic and detecting techniques.
Chinese Multi‐Center Research Collaborative Group on Clinical Diagnosis and Intervention of Auditory Neuropathy +5 more
wiley +1 more source
Case Reports in Cardiology, Volume 2026, Issue 1, 2026.Sudden cardiac death (SCD) is a prevalent and significant health concern which may be preceded by palpitations and presyncope in a young patient. Of the arrhythmogenic causes of SCD, arrhythmogenic cardiomyopathy (ACM) is rare but important with a high morbidity and mortality.
Jasraj Singh +3 more
wiley +1 more source