Isolated double chambered right ventricle as a rare cause of sudden death in infancy

Isolated double-chambered right ventricle (DCRV) is a rare form of congenital heart disorder in which the right ventricle is divided into a high-pressure inlet portion and a low-pressure outlet portion by an anomalous muscle bundle. Rarely, autopsy cases describing this congenital heart disease have...

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Main Authors: W. Thaljawi, M. Belhadj, Y. Chkirben, S. Bouslema, M. Jedidi, T. Masmoudi, M.K Souguir, M.T. Yaâcoubi, M. Ben Dhiab
Format: Article
Language:English
Published: SpringerOpen 2016-12-01
Series:Egyptian Journal of Forensic Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2090536X16300090
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spelling doaj-b7ba82564e0e4017a72795f2cb1ab1e22020-11-25T01:56:01ZengSpringerOpenEgyptian Journal of Forensic Sciences2090-536X2016-12-016450550810.1016/j.ejfs.2016.04.005Isolated double chambered right ventricle as a rare cause of sudden death in infancyW. ThaljawiM. BelhadjY. ChkirbenS. BouslemaM. JedidiT. MasmoudiM.K SouguirM.T. YaâcoubiM. Ben DhiabIsolated double-chambered right ventricle (DCRV) is a rare form of congenital heart disorder in which the right ventricle is divided into a high-pressure inlet portion and a low-pressure outlet portion by an anomalous muscle bundle. Rarely, autopsy cases describing this congenital heart disease have been reported in the world literature. We report the case of a 50-day-old male who died seven days after been suffering from fever and dyspnea. The autopsy revealed essentially an isolated double-chambered right ventricle (DCRV) and an important pulmonary edema. In this paper, we present the first reported case of sudden unanticipated death in infancy due to isolated double-chambered right ventricle.http://www.sciencedirect.com/science/article/pii/S2090536X16300090Sudden deathCongenital heart diseaseDouble chambered right ventricleAutopsy
collection DOAJ
language English
format Article
sources DOAJ
author W. Thaljawi
M. Belhadj
Y. Chkirben
S. Bouslema
M. Jedidi
T. Masmoudi
M.K Souguir
M.T. Yaâcoubi
M. Ben Dhiab
spellingShingle W. Thaljawi
M. Belhadj
Y. Chkirben
S. Bouslema
M. Jedidi
T. Masmoudi
M.K Souguir
M.T. Yaâcoubi
M. Ben Dhiab
Isolated double chambered right ventricle as a rare cause of sudden death in infancy
Egyptian Journal of Forensic Sciences
Sudden death
Congenital heart disease
Double chambered right ventricle
Autopsy
author_facet W. Thaljawi
M. Belhadj
Y. Chkirben
S. Bouslema
M. Jedidi
T. Masmoudi
M.K Souguir
M.T. Yaâcoubi
M. Ben Dhiab
author_sort W. Thaljawi
title Isolated double chambered right ventricle as a rare cause of sudden death in infancy
title_short Isolated double chambered right ventricle as a rare cause of sudden death in infancy
title_full Isolated double chambered right ventricle as a rare cause of sudden death in infancy
title_fullStr Isolated double chambered right ventricle as a rare cause of sudden death in infancy
title_full_unstemmed Isolated double chambered right ventricle as a rare cause of sudden death in infancy
title_sort isolated double chambered right ventricle as a rare cause of sudden death in infancy
publisher SpringerOpen
series Egyptian Journal of Forensic Sciences
issn 2090-536X
publishDate 2016-12-01
description Isolated double-chambered right ventricle (DCRV) is a rare form of congenital heart disorder in which the right ventricle is divided into a high-pressure inlet portion and a low-pressure outlet portion by an anomalous muscle bundle. Rarely, autopsy cases describing this congenital heart disease have been reported in the world literature. We report the case of a 50-day-old male who died seven days after been suffering from fever and dyspnea. The autopsy revealed essentially an isolated double-chambered right ventricle (DCRV) and an important pulmonary edema. In this paper, we present the first reported case of sudden unanticipated death in infancy due to isolated double-chambered right ventricle.
topic Sudden death
Congenital heart disease
Double chambered right ventricle
Autopsy
url http://www.sciencedirect.com/science/article/pii/S2090536X16300090
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