Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome

Introduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor laterally disorder. It is characterized by anomalies of the spleen and other abdominal organs as well as malformations of the heart. Case report: a...

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Main Authors: Melissa Toledo Licourt, Ana Laura Tellez García, Deysi Licourt Otero
Format: Article
Language:Spanish
Published: Universidad de Ciencias Médicas de Pinar del Río 2019-01-01
Series:Universidad Médica Pinareña
Subjects:
Online Access:http://revgaleno.sld.cu/index.php/ump/article/view/329
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spelling doaj-6633c964da6d44abb084c500f5e6404e2020-11-25T02:04:16ZspaUniversidad de Ciencias Médicas de Pinar del RíoUniversidad Médica Pinareña1990-79902019-01-01151148154329Congenital heart disease and inverse situs as a prenatal expression of Ivemark SyndromeMelissa Toledo LicourtAna Laura Tellez GarcíaDeysi Licourt OteroIntroduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor laterally disorder. It is characterized by anomalies of the spleen and other abdominal organs as well as malformations of the heart. Case report: a 15-month-old boy who underwent fetal echocardiography in the 28th week of his fetal development, in the left heart cavity an axis of more than 650 with increase of right cavities, at the aortic valve level a slight decrease in its caliber was observed. Diagnostic impressions are presented as inverse situs, interruption of inferior vena cava and continuation with azygos vein, aortic valvular stenosis and left isomerism. Cesarean delivery was performed at 39 weeks of pregnancy, weight 5080 gr, apgar scoring 9-9. In the abdominal ultrasound the spleen was not defined, the right kidney was malrotated observing also intestinal malrotation. Ivemark Syndrome was the definitive diagnosis. The infant is periodically monitored by a multidisciplinary medical team. Conclusions: at present, it is possible to formulate an early diagnosis of the cardinal signs that involve internal organs such as cardiovascular system, liver, and spleen during prenatal stage to confirm the Ivemark Syndrome, which contributes to the genetic counseling and the multidisciplinary approach in the neonatal stage, avoiding fatal complications and therefore to increase in quality and life expectancy.http://revgaleno.sld.cu/index.php/ump/article/view/329síndrome de heterotaxiacardiopatíasanomalías cardiovascularescardiopatías congénitasheterotaxy syndromeheart diseasescardiovascular abnormalitiesheart defects, congenital
collection DOAJ
language Spanish
format Article
sources DOAJ
author Melissa Toledo Licourt
Ana Laura Tellez García
Deysi Licourt Otero
spellingShingle Melissa Toledo Licourt
Ana Laura Tellez García
Deysi Licourt Otero
Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
Universidad Médica Pinareña
síndrome de heterotaxia
cardiopatías
anomalías cardiovasculares
cardiopatías congénitas
heterotaxy syndrome
heart diseases
cardiovascular abnormalities
heart defects, congenital
author_facet Melissa Toledo Licourt
Ana Laura Tellez García
Deysi Licourt Otero
author_sort Melissa Toledo Licourt
title Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
title_short Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
title_full Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
title_fullStr Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
title_full_unstemmed Congenital heart disease and inverse situs as a prenatal expression of Ivemark Syndrome
title_sort congenital heart disease and inverse situs as a prenatal expression of ivemark syndrome
publisher Universidad de Ciencias Médicas de Pinar del Río
series Universidad Médica Pinareña
issn 1990-7990
publishDate 2019-01-01
description Introduction: Ivemark Syndrome is a rare congenital condition that affects multiple organs of the body; it is classified as a disorder of heterotaxiaor laterally disorder. It is characterized by anomalies of the spleen and other abdominal organs as well as malformations of the heart. Case report: a 15-month-old boy who underwent fetal echocardiography in the 28th week of his fetal development, in the left heart cavity an axis of more than 650 with increase of right cavities, at the aortic valve level a slight decrease in its caliber was observed. Diagnostic impressions are presented as inverse situs, interruption of inferior vena cava and continuation with azygos vein, aortic valvular stenosis and left isomerism. Cesarean delivery was performed at 39 weeks of pregnancy, weight 5080 gr, apgar scoring 9-9. In the abdominal ultrasound the spleen was not defined, the right kidney was malrotated observing also intestinal malrotation. Ivemark Syndrome was the definitive diagnosis. The infant is periodically monitored by a multidisciplinary medical team. Conclusions: at present, it is possible to formulate an early diagnosis of the cardinal signs that involve internal organs such as cardiovascular system, liver, and spleen during prenatal stage to confirm the Ivemark Syndrome, which contributes to the genetic counseling and the multidisciplinary approach in the neonatal stage, avoiding fatal complications and therefore to increase in quality and life expectancy.
topic síndrome de heterotaxia
cardiopatías
anomalías cardiovasculares
cardiopatías congénitas
heterotaxy syndrome
heart diseases
cardiovascular abnormalities
heart defects, congenital
url http://revgaleno.sld.cu/index.php/ump/article/view/329
work_keys_str_mv AT melissatoledolicourt congenitalheartdiseaseandinversesitusasaprenatalexpressionofivemarksyndrome
AT analauratellezgarcia congenitalheartdiseaseandinversesitusasaprenatalexpressionofivemarksyndrome
AT deysilicourtotero congenitalheartdiseaseandinversesitusasaprenatalexpressionofivemarksyndrome
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