[>Femoral bone infarction revealing compound heterozygous SC sickle cell disease in a Moroccan patient].
Infarctus de l´os fémoral révélant une drépanocytose composite SC chez un patient marocain.
Hemoglobinopathy
bone infarction
compound heterozygous SC sickle cell disease
early detection
Journal
The Pan African medical journal
ISSN: 1937-8688
Titre abrégé: Pan Afr Med J
Pays: Uganda
ID NLM: 101517926
Informations de publication
Date de publication:
2020
2020
Historique:
received:
06
04
2020
accepted:
14
04
2020
entrez:
23
11
2020
pubmed:
24
11
2020
medline:
15
1
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 33224427
doi: 10.11604/pamj.2020.36.361.22688
pii: PAMJ-36-361
pmc: PMC7664144
doi:
Types de publication
Case Reports
Langues
fre
Sous-ensembles de citation
IM
Pagination
361Informations de copyright
Copyright: Fatima-Zahrae Bennis et al.
Déclaration de conflit d'intérêts
Les auteurs ne déclarent aucun conflit d´intérêts.
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