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[>Femoral bone infarction revealing compound heterozygous SC sickle cell disease in a Moroccan patient]. | LitMetric

[>Femoral bone infarction revealing compound heterozygous SC sickle cell disease in a Moroccan patient].

Pan Afr Med J

Laboratoire de Biochimie-Toxicologie de l´Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.

Published: January 2021

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664144PMC
http://dx.doi.org/10.11604/pamj.2020.36.361.22688DOI Listing

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