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Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain
Double heterozygosity SC is a major sickle cell syndrome. Its course may be marked by severe or irreversible complications, such as bone infarction. We here report the case of a 17-year-old patient presenting with compound heterozygous SC sickle cell disease following severe knee pain (gonalgia) in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664144/ https://www.ncbi.nlm.nih.gov/pubmed/33224427 http://dx.doi.org/10.11604/pamj.2020.36.361.22688 |
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author | Bennis, Fatima-Zahrae Biaz, Asmae Zkik, Aida Rachid, Achraf Bouhsain, Sanae Dami, Abdellah Samira, Elmachtani Idrissi |
author_facet | Bennis, Fatima-Zahrae Biaz, Asmae Zkik, Aida Rachid, Achraf Bouhsain, Sanae Dami, Abdellah Samira, Elmachtani Idrissi |
author_sort | Bennis, Fatima-Zahrae |
collection | PubMed |
description | Double heterozygosity SC is a major sickle cell syndrome. Its course may be marked by severe or irreversible complications, such as bone infarction. We here report the case of a 17-year-old patient presenting with compound heterozygous SC sickle cell disease following severe knee pain (gonalgia) in order to highlight the risk of delayed diagnosis as well as the need for prevention policies guiding early screening, thus improving patients’ management and prognosis. |
format | Online Article Text |
id | pubmed-7664144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-76641442020-11-20 Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain Bennis, Fatima-Zahrae Biaz, Asmae Zkik, Aida Rachid, Achraf Bouhsain, Sanae Dami, Abdellah Samira, Elmachtani Idrissi Pan Afr Med J Case Report Double heterozygosity SC is a major sickle cell syndrome. Its course may be marked by severe or irreversible complications, such as bone infarction. We here report the case of a 17-year-old patient presenting with compound heterozygous SC sickle cell disease following severe knee pain (gonalgia) in order to highlight the risk of delayed diagnosis as well as the need for prevention policies guiding early screening, thus improving patients’ management and prognosis. The African Field Epidemiology Network 2020-08-28 /pmc/articles/PMC7664144/ /pubmed/33224427 http://dx.doi.org/10.11604/pamj.2020.36.361.22688 Text en Copyright: Fatima-Zahrae Bennis et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bennis, Fatima-Zahrae Biaz, Asmae Zkik, Aida Rachid, Achraf Bouhsain, Sanae Dami, Abdellah Samira, Elmachtani Idrissi Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain |
title | Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain |
title_full | Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain |
title_fullStr | Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain |
title_full_unstemmed | Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain |
title_short | Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain |
title_sort | infarctus de l´os fémoral révélant une drépanocytose composite sc chez un patient marocain |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664144/ https://www.ncbi.nlm.nih.gov/pubmed/33224427 http://dx.doi.org/10.11604/pamj.2020.36.361.22688 |
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