Results 11 to 20 of about 570,477 (309)

Restrictive Cardiomyopathy in a Child [PDF]

Pediatrics and Neonatology, 2008
Restrictive cardiomyopathy in young children is rare and carries a poor prognosis. We report an 18-month-old girl with poor feeding and abdominal distension. Except for hepatomegaly, no other gastrointestinal abnormalities were found. She had normalsized
Shan-Miao Lin, Haw-Kwei Hwang, Ming-Ren Chen   +2 more
doaj   +4 more sources

Restrictive Cardiomyopathy [PDF]

Postgraduate Medical Journal, 1986
Restrictive obliterative cardiomyopathy, with emphasis on amyloid infiltration of the heart, is discussed. The presence of right-sided failure associated with low-voltage electrocardiographic complexes may simulate constrictive pericarditis.
Garcia, Remigio, Alam, Mohsin
core   +5 more sources

Desmin-related cardiomyopathy presenting as restrictive cardiomyopathy: A case report with review of literature

Journal of the Practice of Cardiovascular Sciences, 2016
Isolated cardiac involvement due to deposition of desmin is a rare cause of restrictive cardiomyopathy due to pathogenic mutation in desmin related genes.
Kalpana Kumari, Sudheer Arava, T C Nag, Ruma Ray   +3 more
doaj   +2 more sources

Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype [PDF]

Cardiogenetics, 2012
Restrictive cardiomyopathy (RCM) is defined on the basis of the haemodynamic finding of restrictive ventricular physiology. However, restrictive ventricular pathophysiology is also a feature of other subtypes of cardiomyopathy, including hypertrophic ...
Juan Pablo Kaski, Elena Biagini, Massimo Lorenzini, Claudio Rapezzi, Perry Elliott   +4 more
doaj   +2 more sources

Restrictive cardiomyopathy. Report of seven cases

Acta Pediátrica de México, 2014
Restrictive cardiomyopathy is a disease characterized by ventricular diastolic failure with elevation of end-dyastolic pressure and preserved systolic function.
Fonseca Sánchez Luis Alfonso, Camacho Reyes Laura, Bobadilla Aguirre Alfredo   +2 more
doaj   +2 more sources

A Case of Rare Inherited Restrictive Cardiomyopathy With Severe Biatrial Enlargement

JACC: Case Reports, 2019
We describe a case of inherited restrictive cardiomyopathy in a patient presenting with severe biatrial enlargement. We review the evaluation and management of restrictive cardiomyopathy with a focus on genetic etiologies.
Navid A. Nafissi, MD, Marat Fudim, MD, Carmelo A. Milano, MD, Paul B. Rosenberg, MD, Adam D. DeVore, MD, MHS, Richa Agarwal, MD   +5 more
doaj   +2 more sources

Prognosis of pediatric restrictive cardiomyopathy: more severe in sarcomeric variants [PDF]

Frontiers in Genetics
Restrictive cardiomyopathy (RCM) is the most severe type of cardiomyopathy in children with a very poor prognosis. RCM is often diagnosed between 6 and 10 years old and is predominantly of genetic origin. We conducted a retrospective study of 53 patients.
Catherine Gardin, Pierre-Emmanuel Michels, Elena Panaioli, Elise Daire, Flavie Ader, Flavie Ader, Flavie Ader, Sophie Malekzadeh-Milani, Damien Bonnet, Diala Khraiche   +9 more
doaj   +2 more sources

Early-onset restrictive cardiomyopathy with life-threatening arrhythmia caused by a homozygous desmin mutation: a case report [PDF]

BMC Pediatrics
Restrictive cardiomyopathy (RCM) is a rare cardiac disease characterized by the predominance of severe diastolic dysfunction, normal or mildly increased ventricular wall thickness, and either normal or mildly reduced ejection fraction.
Tianjiao Wang, Weina Zhao, Lifang Wu, Qinlai Ying, Wen Zhu, Yiqun Teng, Xiaolin Liu   +6 more
doaj   +2 more sources

Restrictive cardiomyopathy

, 2018
Restrictive cardiomyopathy (RCM) is an uncommon myocardial disease, characterized by impaired filling of the ventricles in the presence of normal wall thickness and systolic function.
Jens Mogensen
core   +4 more sources

Engineered cardiac tissue model of restrictive cardiomyopathy for drug discovery

Cell Reports Medicine, 2023
Summary Restrictive cardiomyopathy (RCM) is defined as increased myocardial stiffness and impaired diastolic relaxation leading to elevated ventricular filling pressures. Human variants in filamin C (FLNC) are linked to a variety of cardiomyopathies, and
Bryan Z. Wang, Trevor R. Nash, Xiaokan Zhang, J. Rao, L. Abriola, Youngbin Kim, S. Zakharov, Michael Kim, Lori J. Luo, Margreet Morsink, Bo-Hao Liu, Roberta I. Lock, Sharon Fleischer, M. Tamargo, Michael S Bohnen, C. Welch, Wendy K. Chung, S. Marx, Y. Surovtseva, G. Vunjak-Novakovic, B. Fine   +20 more
semanticscholar   +1 more source