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由右心室心肌致密化不全引起的短暂性产后心力衰竭。

Transient postnatal heart failure caused by noncompaction of the right ventricular myocardium.

作者信息

Hruda J, Sobotka-Plojhar M A, Fetter W P F

机构信息

Department of Pediatric Cardiology, VU University Medical Center, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.

出版信息

Pediatr Cardiol. 2005 Jul-Aug;26(4):452-4. doi: 10.1007/s00246-004-0752-z.

DOI:10.1007/s00246-004-0752-z
PMID:16374698
Abstract

Isolated noncompaction of the ventricular myocardium is a cardiomyopathy influencing almost exclusively the left ventricle in children and adults. We report a case of a neonate presenting with right ventricular failure caused by a noncompaction of the right ventricle. However, later course of the disease demonstrated biventricular involvement. Right ventricular noncompaction can be a cause of early postnatal right ventricular failure.

摘要

孤立性心室心肌致密化不全是一种几乎仅影响儿童和成人左心室的心肌病。我们报告一例新生儿因右心室致密化不全导致右心衰竭的病例。然而,疾病的后期病程显示双心室受累。右心室致密化不全可能是出生后早期右心衰竭的一个原因。

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Echocardiography. 2003 May;20(4):379-83. doi: 10.1046/j.1540-8175.2003.03045.x.
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Isolated non-compaction of the ventricular myocardium: prenatal diagnosis and natural history.
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Korean Circ J. 2015 Sep;45(5):439-41. doi: 10.4070/kcj.2015.45.5.439. Epub 2015 Jun 25.
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Right ventricular obstructive hypertrophic cardiomyopathy in primary myo-adenylate deaminase deficiency.
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The intercellular organization of the two muscular systems in the adult salmonid heart, the compact and the spongy myocardium.成鲑鱼心脏中两种肌肉系统,即致密心肌和海绵心肌的细胞间组织。
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