Literature DB >> 19838476

Echocardiographic features of non-compaction cardiomyopathy: missed and misdiagnosed disease.

Francisco Martínez-Baca López1, Rosa Marisol Alonso Bravo, Domingo Arturo Rodríguez Huerta.   

Abstract

Non-compaction cardiomyopathy is a rare disease, anatomically characterized by a prominent trabecular pattern and deep intertrabecular recesses. Its clinical manifestations include severe left ventricular dysfunction, arrhythmias, systemic embolism, and sudden death. In this report, two cases of patients of different ages with non-compaction cardiomyopathy are described: a male schoolboy whose pathology was associated with mitral stenosis and regurgitation and a 50-year-old female with history of high blood pressure and cardiac failure.

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Year:  2009        PMID: 19838476     DOI: 10.1590/s0066-782x2009000800024

Source DB:  PubMed          Journal:  Arq Bras Cardiol        ISSN: 0066-782X            Impact factor:   2.000


  3 in total

1.  Myopathy should determine the anesthetic management in left ventricular hypertrabeculation/noncompaction.

Authors:  J Finsterer; C Stöllberger
Journal:  Heart Lung Vessel       Date:  2014

Review 2.  Pediatric cardiomyopathies: causes, epidemiology, clinical course, preventive strategies and therapies.

Authors:  Steven E Lipshultz; Thomas R Cochran; David A Briston; Stefanie R Brown; Peter J Sambatakos; Tracie L Miller; Adriana A Carrillo; Liat Corcia; Janine E Sanchez; Melissa B Diamond; Michael Freundlich; Danielle Harake; Tamara Gayle; William G Harmon; Paolo G Rusconi; Satinder K Sandhu; James D Wilkinson
Journal:  Future Cardiol       Date:  2013-11

3.  Knockout of SRC-1 and SRC-3 in Mice Decreases Cardiomyocyte Proliferation and Causes a Noncompaction Cardiomyopathy Phenotype.

Authors:  Xian Chen; Li Qin; Zhaoliang Liu; Lan Liao; James F Martin; Jianming Xu
Journal:  Int J Biol Sci       Date:  2015-07-15       Impact factor: 6.580

  3 in total

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