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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...

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Autores principales: Bennis, Fatima-Zahrae, Biaz, Asmae, Zkik, Aida, Rachid, Achraf, Bouhsain, Sanae, Dami, Abdellah, Samira, Elmachtani Idrissi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
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.
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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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