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Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature

Ballantyne syndrome or preeclampsia (Mirror syndrome) is a rare clinical entity. Ethiopathogenesis is still poorly elucidated. Diagnosis must be suspected in patients with maternal edematous syndrome associated with fetal anasarca. Guarded fetal prognosis can be associate with strong maternal morbid...

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Autores principales: Mangoub, Fatima El, Bouhou, Rachid Ait, Idri, Zakaria, Kouach, Jaouad, Guelzim, Khalid, Rahali, Driss Moussaoui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295295/
https://www.ncbi.nlm.nih.gov/pubmed/30574257
http://dx.doi.org/10.11604/pamj.2018.30.238.15296
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author Mangoub, Fatima El
Bouhou, Rachid Ait
Idri, Zakaria
Kouach, Jaouad
Guelzim, Khalid
Rahali, Driss Moussaoui
author_facet Mangoub, Fatima El
Bouhou, Rachid Ait
Idri, Zakaria
Kouach, Jaouad
Guelzim, Khalid
Rahali, Driss Moussaoui
author_sort Mangoub, Fatima El
collection PubMed
description Ballantyne syndrome or preeclampsia (Mirror syndrome) is a rare clinical entity. Ethiopathogenesis is still poorly elucidated. Diagnosis must be suspected in patients with maternal edematous syndrome associated with fetal anasarca. Guarded fetal prognosis can be associate with strong maternal morbidity. This highlights the role of early diagnosis based on cause detection aimed to establish an antenatal treatment that could improve maternofoetal prognosis. We report and discuss in the light of a literature review a case of a probable Ballantyne syndrome secondary to fetal malformative syndrome complicated by eclampsia in the mother.
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spelling pubmed-62952952018-12-20 Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature Mangoub, Fatima El Bouhou, Rachid Ait Idri, Zakaria Kouach, Jaouad Guelzim, Khalid Rahali, Driss Moussaoui Pan Afr Med J Case Report Ballantyne syndrome or preeclampsia (Mirror syndrome) is a rare clinical entity. Ethiopathogenesis is still poorly elucidated. Diagnosis must be suspected in patients with maternal edematous syndrome associated with fetal anasarca. Guarded fetal prognosis can be associate with strong maternal morbidity. This highlights the role of early diagnosis based on cause detection aimed to establish an antenatal treatment that could improve maternofoetal prognosis. We report and discuss in the light of a literature review a case of a probable Ballantyne syndrome secondary to fetal malformative syndrome complicated by eclampsia in the mother. The African Field Epidemiology Network 2018-07-31 /pmc/articles/PMC6295295/ /pubmed/30574257 http://dx.doi.org/10.11604/pamj.2018.30.238.15296 Text en © Fatima El Mangoub et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mangoub, Fatima El
Bouhou, Rachid Ait
Idri, Zakaria
Kouach, Jaouad
Guelzim, Khalid
Rahali, Driss Moussaoui
Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature
title Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature
title_full Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature
title_fullStr Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature
title_full_unstemmed Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature
title_short Syndrome de Ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature
title_sort syndrome de ballantyne compliqué d’eclampsie: à propos d’un cas et revue de la littérature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295295/
https://www.ncbi.nlm.nih.gov/pubmed/30574257
http://dx.doi.org/10.11604/pamj.2018.30.238.15296
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