ⓘ Noncompaction cardiomyopathy

                                     

ⓘ Noncompaction cardiomyopathy

Non-compaction cardiomyopathy, is a rare congenital cardiomyopathy that affects both children and adults. It results from the failure of myocardial development during embryogenesis.

In the course of development, a large part of the heart muscle spongy mesh of interlaced fibers of the myocardium. As usual in the development process, these trabeculated structures undergo significant compaction that transforms them from spongy to solid. This process is particularly noticeable in the ventricles especially in the left ventricle. Non-compact left ventricular myocardium, cardiomyopathy results when there is failure of this process of compaction. Because the consequence of non-compact this is particularly noticeable in the left ventricle, also called left ventricular non-compacted myocardium of the left ventricle. Other hypotheses and models have been proposed, none of which is as widely accepted as a model of non-compacted myocardium of the left ventricle.

The symptoms vary greatly in severity. Most of them are the result of poor pumping performance of the heart. The disease may be associated with other heart problems and body.

                                     
  • diseases such as hypertrophic cardiomyopathy dilated cardiomyopathy noncompaction cardiomyopathy and arrhythmogenic cardiomyopathy also known as arrhythmogenic
  • multi - system disorder include: cardiomyopathy dilated or hypertrophic, possibly with left ventricular noncompaction and or endocardial fibroelastosis
  • myofibrillar myopathy, dilated cardiomyopathy arrhythmogenic right ventricular cardiomyopathy noncompaction cardiomyopathy and muscular dystrophy. The
  • in ITGA7 have been associated with congenital myopathies and noncompaction cardiomyopathy and altered expression levels of alpha - 7 integrin have been
  • New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy anemia, ataxia, and male genital anomalies Pediatric Research
  • ACE inhibitors Respiratory aid Physical therapy Laminopathies Noncompaction cardiomyopathy Brown SC, Piercy RJ, Muntoni F, Sewry CA December 2008 Investigating
  • Barth syndrome, dilated cardiomyopathy DCM hypertrophic DCM, endocardial fibroelastosis, left ventricular noncompaction LVNC breast cancer, papillary
  • missense mutation has been associated with Hypertrophic Cardiomyopathy and Left Ventricular Noncompaction Another mutation has in the ACTC1 gene has been associated
  • lead to various forms of cardiomyopathies such as dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy In patients with isolated
  • honors. Following his freshman campaign, Boyd was diagnosed with noncompaction cardiomyopathy He was forced to sit out the 2009 10 season with a medical redshirt
  • cause of dilated cardiomyopathy including aortic insufficiency, nonischemic dilated cardiomyopathy and Noncompaction cardiomyopathy Because the papillary