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The NAXCARE (NAXos disease and Cardiocutaneous Assessment and Registry for Evaluation) is a global initiative designed to collect, store, and analyze clinical outcomes data on patients with Naxos disease and related cardiocutaneous syndromes (CCS). This registry aims to fill the gaps in clinical knowledge, enhance treatment approaches, and improve patient outcomes by systematically documenting disease progression, genetic profiles, and patient care pathways. The following methodology outlines the registry's design, data collection protocols, management, security measures, and anticipated contributions to research and clinical practice.
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http://dx.doi.org/10.1016/j.hjc.2025.04.004 | DOI Listing |
Diagnostics (Basel)
June 2025
Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania.
The electrocardiogram (ECG) remains a cornerstone of modern cardiology, providing rapid, non-invasive, and widely accessible diagnostic insights. While ECG interpretation is an essential skill for clinicians, certain patterns can be subtle or atypical, posing diagnostic challenges. In our previous review (doi.
View Article and Find Full Text PDFHellenic J Cardiol
April 2025
Centre for Heart Muscle Disease, UCL Institute of Cardiovascular Science, London, UK.
The NAXCARE (NAXos disease and Cardiocutaneous Assessment and Registry for Evaluation) is a global initiative designed to collect, store, and analyze clinical outcomes data on patients with Naxos disease and related cardiocutaneous syndromes (CCS). This registry aims to fill the gaps in clinical knowledge, enhance treatment approaches, and improve patient outcomes by systematically documenting disease progression, genetic profiles, and patient care pathways. The following methodology outlines the registry's design, data collection protocols, management, security measures, and anticipated contributions to research and clinical practice.
View Article and Find Full Text PDFCardiol Young
May 2025
Department of Pediatric Cardiology, University of Health Sciences Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Introduction: Carvajal syndrome, a rare autosomal recessive disorder caused by mutations in the gene, is characterised by woolly hair, palmoplantar keratoderma, and left ventricular dilated cardiomyopathy. Although less frequently reported, noncompaction cardiomyopathy can co-occur, further complicating the clinical picture. Early diagnosis and management are crucial due to the high risk of progressive heart failure and sudden cardiac death in affected individuals.
View Article and Find Full Text PDFHellenic J Cardiol
April 2025
Paediatric Clinic, Hora Naxos 84300, Greece. Electronic address:
Clin Exp Dermatol
July 2025
Department of Dermatology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.