Relevant bibliographies by topics / Abdominal ectopia cordis

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Academic literature on the topic 'Abdominal ectopia cordis'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Abdominal ectopia cordis"

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Rahman, Md Hamidur, Mahmuda Hassan, Kona Chowdhury, and Abdul Quddus. "Ectopia Cordis." Journal of Nepal Paediatric Society 36, no. 2 (2016): 184–87. http://dx.doi.org/10.3126/jnps.v36i2.14807.

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Ectopia Cordis is a rare congenital anomaly characterized by partial or complete displacement of the heart outside the thoracic cavity. Usually ectopiacordis is associated with other multiple anomalies and intra cardiac defects. The five main ectopic positions are adjacent to the thorax approximately 60%, abdominal is 15-30%, thoraco-abdominal is 7-18%, cervical is about 3% and least is the cervicothoracic. We are reporting a case of ectopiacordis of abdominal type. This is the first reported abdominal ectopia cordis case in Bangladesh.
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Caliskan, N., E. Forrez, N. Van Roy, and S. Roels. "Abdominal ectopia cordis in an aborted calf without chromosomal aberrations." Vlaams Diergeneeskundig Tijdschrift 90, no. 4 (2021): 178–81. http://dx.doi.org/10.21825/vdt.v90i4.20710.

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Ectopia cordis is a rare congenital heart disease characterized by partial or complete displacement of the heart out of the thoracic cavity. Apart from cattle, the condition has also been described in humans and is frequently associated with Cantrell’s pentalogy. It is classified into five types: cervical, cervicothoracic, thoracic, abdominal and thoracoabdominal. The prognosis is poor and ectopia cordis may be linked to the presence of unbalanced chromosome alterations. In this report, a case of abdominal ectopia cordis is described in an aborted calf, in which no unbalanced structural chromo
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3

Kabbani, Mohamed S., Khalid Rasheed, Mohammed S. Mallick, Hannan Abu-Hassan, and Saad Al-Yousef. "Thoraco-Abdominal Ectopia Cordis: Case Report." Annals of Saudi Medicine 22, no. 5-6 (2002): 366–68. http://dx.doi.org/10.5144/0256-4947.2002.366.

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4

García-Muñoz, Iván, Efrén Flores-Álvarez, Javier González-Peña, Miguel Ángel Chagolla-Santillán, Iliana Acevedo-Bañuelos, and Elena Rocha-Peña. "Ectopia Cordis: reporte de un caso." Lux Médica 10, no. 30 (2015): 43–47. http://dx.doi.org/10.33064/30lm2015757.

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La ectopia cordis es una posición anómala en la cual el corazón se ubica de forma parcial o total fuera de la cavidad torácica. Su tasa de incidencia es extremadamente baja, representa el 0.5% de las cardiopatías de tipo congénito. El corazón puede ubicarse en la región cervical, torácica, abdominal o torácico-abdominal. El pronóstico a corto plazo es malo debido a las malformaciones asociadas. Presentamos el caso de una paciente recién nacida, a quien se le diagnosticó malformación congénita cardíaca de tipo ectopia cordis desde la gestación, al nacimiento se confirmó un defecto del tipo torá
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Bhatnagar, V., AK Singal, and P. Balamourougane. "Primary closure of thoraco-abdominal ectopia cordis." Journal of Indian Association of Pediatric Surgeons 11, no. 4 (2006): 250. http://dx.doi.org/10.4103/0971-9261.29613.

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Ashwin, V. Apte. "Thoraco-Abdominal Ectopia Cordis: A Rare Entity. Case Report and Review of Literature." PJSR 1, no. 1 (2008): 31–33. https://doi.org/10.5281/zenodo.8245644.

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Ectopia cordis is a rare congenital abnormality characterised by partial or complete displacement of the heart outside the thoracic cavity. It can be associated with other congenital abnormalities. The present case was a two hours old male child and a product of non-consanguineous marriage. Child had thoraco-abdominal ectopia cordis. Condition of child detoriated rapidly and succumbed before any investigation and surgical intervention could be performed.
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7

Pappalardo, Elisa, Ferdinando Antonio Gulino, Carla Ettore, Francesco Cannone, and Giuseppe Ettore. "Body Stalk Anomaly Complicated by Ectopia Cordis: First-Trimester Diagnosis of Two Cases Using 2- and 3-Dimensional Sonography." Journal of Clinical Medicine 12, no. 5 (2023): 1896. http://dx.doi.org/10.3390/jcm12051896.

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Introduction: Body stalk anomaly is a severe defect of the abdominal wall, characterized by the evisceration of abdominal organs and, in more severe cases, thoracic organs as well. The most serious condition in a body stalk anomaly may be complicated by ectopia cordis, an abnormal location of the heart outside the thorax. The aim of this scientific work is to describe our experience with the prenatal diagnosis of ectopia cordis as part of the first-trimester sonographic screening for aneuploidy. Methods: We report two cases of body stalk anomalies complicated by ectopia cordis. The first case
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8

Andrianjakamanana, Tolojanahary Herizo, Alice Razafindrahova Patricia Alice Patricia, Christian Tomboravo, et al. "Ectopia Cordis Thoraco-Abdominal Diagnosed with Antenatal Ultrasound." American Journal of Medical Science and Innovation 1, no. 1 (2023): 1–3. https://doi.org/10.54536/ajmsi.v2i1.1157.

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In this article we report a case of ectopia cordis, which is a rare congenital malformation characterized by an extra-thoracic position of the heart. This is the thoracic-abdominal form, of antenatal discovery on a pregnancy of 35 weeks and 03 days, during an obstetric ultrasound monitoring pregnancy during the third trimester of pregnancy, made at the University Hospital Professor Zafisaona Gabriel, Mahajanga Madagascar. The objective of this work is to report the antenatal ultrasound diagnostic elements of this rare malformation. Ultrasound plays an important role in antenatal diagnosis and
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9

Shrestha, Ramesh, S. Chhetri, MC Regmi, and P. Basnet. "Ectopia Cordis: a Rare Congenital Condition." Nepal Journal of Obstetrics and Gynaecology 12, no. 1 (2018): 59–61. http://dx.doi.org/10.3126/njog.v12i1.18984.

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Ectopia cordis is a rare congenital malformation and only few cases have been reported in literature previously. It is defined as the complete or partial evisceration of heart outside the thoracic cavity through the sternal defect. Most cases are sporadic. The classical presentation for the antenatal diagnosis on ultrasonography is a pulsating heart out of the thoracic cavity with absent chest wall.We reported three cases of ectopia cordis in the last one and half year in our institute. Two of them were diagnosed on ultrasound and the third case terminated for meningocele with severe oligohydr
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10

Muhammad, Umar Nisar, Sikander Samer, Akhtar Nadeem, Atanasova Maria-Desislava, and Inkov Ivan. "Pentalogy of Cantrell or Cantrell Syndrome: One in a million disease." International Journal of Medical Reviews and Case Reports 3, no. 7 (2019): 482–85. https://doi.org/10.5455/IJMRCR.Pantalogy-Cantrell-Cantrell-Syndrome.

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Introduction: Pentalogy of Cantrell (PS) or Cantrell Sydrome (CS), first described by Cantrell in 1958, is a rare congenital anomaly characterized by defect in lower sternum, anterior abdominal wall defect, defect in anterior diaphragm, ectopia cordis and congenital heart disease. Case Report: A 12 hours female neonate born to full term primigravida was reffered to us with her heart lying outside the chest and an omphalocele as well. Baby had complete thoracic ectopia cordis, midline anterior thoraco-abdominal wall defect through with liver was protruding which was covered by a membrane. Stern
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Conference papers on the topic "Abdominal ectopia cordis"

1

Guimarães, Julia Goes, Kelvin Cleyton Ribeuro, Guilherme Ribeiro Ramires de Jesús, Ana Elisa Rodrigues Baião, and Fernando Maia Peixoto Filho. "Pentalogia de Cantrell: um relato de caso." In 45º Congresso da SGORJ XXIV Trocando Ideias. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/jbg-0368-1416-20211311186.

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Introdução: A pentalogia de Cantrell (PC) é uma forma rara de defeito da parede abdominal que consiste na associação de cinco malformações maiores: anormalidade na linha média da parede abdominal superior, defeito esternal, defeito diafragmático, defeito pericárdico e anomalias congênitas do coração. Entre elas, os achados mais comuns são onfalocele e defeito do septo atrioventricular. Sua incidência varia de 1:65.000 a 1:200.000, porém sua etiologia é incerta. A teoria mais aceita é uma alteração no desenvolvimento fetal 18-21 dias após a concepção, quando há alteração na migração das estrutu
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Journal articles
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