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Clinical Presentation and Therapy of Cardiomyopathies.
Haas, Nikolaus A; Driscoll, David J; Rickert-Sperling, Silke.
Affiliation
  • Haas NA; Department of Pediatric Cardiology and Intensive Care, Ludwig Maximilians University, Munich, Germany. Nikolaus.haas@med.uni-muenchen.de.
  • Driscoll DJ; Division of Pediatric Cardiology, Department of Pediatrics, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Rickert-Sperling S; Cardiovascular Genetics, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Adv Exp Med Biol ; 1441: 965-976, 2024.
Article de En | MEDLINE | ID: mdl-38884764
ABSTRACT
Cardiomyopathies are a group of diseases that primarily affect the heart muscle, leading to mechanical or electrical dysfunction of the heart. They can be categorized into primary and secondary forms. Primary cardiomyopathies can be further classified as congenital, acquired, or mixed. In terms of the heart muscle itself, there are five distinct types of cardiomyopathies hypertrophic cardiomyopathy, dilated or congestive cardiomyopathy, restrictive cardiomyopathy, arrhythmogenic (right ventricular) dysplasia, and noncompaction cardiomyopathy. While cardiomyopathies primarily affect the heart, they can also have systemic manifestations, impacting other organs and potentially causing progressive debilitation, heart failure, or even death.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Cardiomyopathies Limites: Humans Langue: En Journal: Adv Exp Med Biol Année: 2024 Type de document: Article Pays d'affiliation: Allemagne

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Cardiomyopathies Limites: Humans Langue: En Journal: Adv Exp Med Biol Année: 2024 Type de document: Article Pays d'affiliation: Allemagne