NDLI: Atrésie intestinale iléale: diagnostic anténatale et prise en charge

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Atrésie intestinale iléale: diagnostic anténatale et prise en charge

Content Provider	Semantic Scholar
Author	Dhibou, Hanane Bassir, Ahlam Sami, Nadia Boukhanni, Lahcen Fakhir, Bouchra Asmouki, Hamid Soummani, Abderraouf
Copyright Year	2016
Abstract	L’atrésie iléale est une malformation congénitale rare, elle constitue une faible part avec une incidence de 1 pour 5000 cas. Elle peut être suspectée et diagnostiqué échographiquement à la fin du deuxième et troisième trimestre. La concertation obstétrico-chirurgicale constitue ici la clé du succès. Eliminer une maladie générale à mauvais pronostic, lutter contre la prématurité et confier l’enfant immédiatement au chirurgien sont les objectifs principaux à réaliser. L'intervention chirurgicale va préciser le type de l'atrésie, son siège, son caractère unique ou multiple et sa longueur dont l’acte chirurgical dépend de l’étiologie. Il nous a paru intéressant de vous documenter un cas clinique d’atrésie iléale de diagnostic anténatal. Pan African Medical Journal. 2016; 24:240 doi:10.11604/pamj.2016.24.240.9807 This article is available online at: http://www.panafrican-med-journal.com/content/article/24/240/full/ © Hanane Dhibou et al. The Pan African Medical Journal ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Pan African Medical Journal – ISSN: 19378688 (www.panafrican-med-journal.com) Published in partnership with the African Field Epidemiology Network (AFENET). (www.afenet.net) Case report Open Access
Starting Page	723
Ending Page	726
Page Count	4
File Format	PDF HTM / HTML
PubMed reference number	5075440
Volume Number	24
Language	English
Access Restriction	Open
Subject Keyword	Allergy Unit Amino acidemia disorder suspected:Prid:Pt:Bld.dot:Nom Arnold Chiari Malformation Deformity Ephrin Type-B Receptor 1, human Gilles de la Tourette syndrome Incidence matrix International Standard Serial Number License Linear algebra Scientific Publication Windows NT
Content Type	Text
Resource Type	Article

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