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“Sickle cell trait and haemophilia: a rare association”
In this paper we analyze the combination of HbAS disease and haemophilia A must be exceedingly rare. Because of this rarity we report the case of two brothers with sickle cell trait and major haemophilia A. We conclude that it is about a post-circumcision bleeding due to major hemophilia A associate...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987143/ https://www.ncbi.nlm.nih.gov/pubmed/29875973 http://dx.doi.org/10.11604/pamj.2018.29.92.14551 |
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author | El Maataoui, Hayat Fahi, Amina Oukkache, Bouchra |
author_facet | El Maataoui, Hayat Fahi, Amina Oukkache, Bouchra |
author_sort | El Maataoui, Hayat |
collection | PubMed |
description | In this paper we analyze the combination of HbAS disease and haemophilia A must be exceedingly rare. Because of this rarity we report the case of two brothers with sickle cell trait and major haemophilia A. We conclude that it is about a post-circumcision bleeding due to major hemophilia A associated to sickle cell AS, this association was a systematic discovery. |
format | Online Article Text |
id | pubmed-5987143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-59871432018-06-06 “Sickle cell trait and haemophilia: a rare association” El Maataoui, Hayat Fahi, Amina Oukkache, Bouchra Pan Afr Med J Case Report In this paper we analyze the combination of HbAS disease and haemophilia A must be exceedingly rare. Because of this rarity we report the case of two brothers with sickle cell trait and major haemophilia A. We conclude that it is about a post-circumcision bleeding due to major hemophilia A associated to sickle cell AS, this association was a systematic discovery. The African Field Epidemiology Network 2018-01-30 /pmc/articles/PMC5987143/ /pubmed/29875973 http://dx.doi.org/10.11604/pamj.2018.29.92.14551 Text en © Hayat El Maataoui 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 El Maataoui, Hayat Fahi, Amina Oukkache, Bouchra “Sickle cell trait and haemophilia: a rare association” |
title | “Sickle cell trait and haemophilia: a rare association” |
title_full | “Sickle cell trait and haemophilia: a rare association” |
title_fullStr | “Sickle cell trait and haemophilia: a rare association” |
title_full_unstemmed | “Sickle cell trait and haemophilia: a rare association” |
title_short | “Sickle cell trait and haemophilia: a rare association” |
title_sort | “sickle cell trait and haemophilia: a rare association” |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987143/ https://www.ncbi.nlm.nih.gov/pubmed/29875973 http://dx.doi.org/10.11604/pamj.2018.29.92.14551 |
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