Afibrinogénémie congénitale: à propos d’une observation

Afibrinogenemia is a rare dyscrasia characterized by a congenital fibrinogen deficiency It is transmitted in an autosomal recessive manner. Hemorrhagic manifestations are variable and can be life-threatening. A little more than 250 cases have been published up till now. We here report a new case of...

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Autores principales: Assani, Karim, Karboubi, Lamya, Dakhama, Badr Sououd Benjelloun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337292/
https://www.ncbi.nlm.nih.gov/pubmed/28293349
http://dx.doi.org/10.11604/pamj.2016.25.233.10754
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author Assani, Karim
Karboubi, Lamya
Dakhama, Badr Sououd Benjelloun
author_facet Assani, Karim
Karboubi, Lamya
Dakhama, Badr Sououd Benjelloun
author_sort Assani, Karim
collection PubMed
description Afibrinogenemia is a rare dyscrasia characterized by a congenital fibrinogen deficiency It is transmitted in an autosomal recessive manner. Hemorrhagic manifestations are variable and can be life-threatening. A little more than 250 cases have been published up till now. We here report a new case of congenital afibrinogenemia in a 3 1/2-year old child hospitalized for medium abundance hematemesis. This case study aims to highlight numerous aspects of this condition from a clinical, biological, genetic and therapeutic points of view.
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spelling pubmed-53372922017-03-14 Afibrinogénémie congénitale: à propos d’une observation Assani, Karim Karboubi, Lamya Dakhama, Badr Sououd Benjelloun Pan Afr Med J Case Report Afibrinogenemia is a rare dyscrasia characterized by a congenital fibrinogen deficiency It is transmitted in an autosomal recessive manner. Hemorrhagic manifestations are variable and can be life-threatening. A little more than 250 cases have been published up till now. We here report a new case of congenital afibrinogenemia in a 3 1/2-year old child hospitalized for medium abundance hematemesis. This case study aims to highlight numerous aspects of this condition from a clinical, biological, genetic and therapeutic points of view. The African Field Epidemiology Network 2016-12-09 /pmc/articles/PMC5337292/ /pubmed/28293349 http://dx.doi.org/10.11604/pamj.2016.25.233.10754 Text en © Karim Assani 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
Assani, Karim
Karboubi, Lamya
Dakhama, Badr Sououd Benjelloun
Afibrinogénémie congénitale: à propos d’une observation
title Afibrinogénémie congénitale: à propos d’une observation
title_full Afibrinogénémie congénitale: à propos d’une observation
title_fullStr Afibrinogénémie congénitale: à propos d’une observation
title_full_unstemmed Afibrinogénémie congénitale: à propos d’une observation
title_short Afibrinogénémie congénitale: à propos d’une observation
title_sort afibrinogénémie congénitale: à propos d’une observation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337292/
https://www.ncbi.nlm.nih.gov/pubmed/28293349
http://dx.doi.org/10.11604/pamj.2016.25.233.10754
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AT karboubilamya afibrinogenemiecongenitaleaproposduneobservation
AT dakhamabadrsououdbenjelloun afibrinogenemiecongenitaleaproposduneobservation

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