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Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
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Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
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Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
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Right Heart Catheterization: An OverviewRight heart catheterization is an invasive diagnostic procedure that measures right-sided cardiac and pulmonary artery pressures, calculates cardiac output, and identifies intracardiac shunts. It provides detailed hemodynamic data essential for diagnosing and managing various cardiovascular conditions, such as pulmonary hypertension.Access SitesCommon access sites for right heart catheterization include the internal jugular vein in the neck region, the...
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Síndrome del corazón izquierdo hipoplásico con septo auricular intacto o restrictivo: un informe del Registro

David W Jantzen1, Anita J Moon-Grady2, Shaine A Morris2

  • 1From C.S. Mott Children's Hospital, University of Michigan, Ann Arbor (D.W.J., C.G.F., S.K.G.); University of California-San Francisco (A.J.M.-G.); Baylor College of Medicine, Houston, TX (S.A.M.); Nationwide Children's Hospital, Columbus, OH (A.K.A.); University of Bonn, Germany (C.B., U.H.); Perinatal Cardiology Clinic, Medical University of Warsaw, Poland (J.D.); Children's Hospital of Wisconsin, Milwaukee (M.F.); University Hospital Bonn, Germany (U.G.); Hospital for Sick Children, Toronto, Ontario, Canada (E.J.); Florida International University, Miami (E.V.K., R.A.Q.); Boston Children's Hospital, MA (A.C.M.); Evelina London Children's Hospital, United Kingdom (O.M.); Technische Universität München, Germany (R.O.); Leiden University Medical Center, Netherlands (D.O.); Hospital do Coração, São Paolo, Brazil (C.A.P., S.R.P., F.P.); and Mount Sinai Hospital, Toronto, Ontario, Canada (G.R.). jantzen@uic.edu.

Circulation
|September 3, 2017
PubMed
Resumen

No abstract available in PubMed .

Palabras clave:
Septoestomía auricularecocardiografíalas terapias fetalesdefectos cardíacos, congénitosSíndrome hipoplástico del corazón izquierdo

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