Manifestations of HbSE sickle cell disease: a systematic review

BACKGROUND: Sickle cell disease (SCD) is commonly encountered in Africa and Middle Eastern countries. The causative mutation in the gene encoding the hemoglobin subunit β (HBB) leads to various genotypic variants of the disease. This results in varied phenotypes, with a spectrum of complications, fr...

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Detalles Bibliográficos
Autores principales: Khamees, Ibrahim, Ata, Fateen, Choudry, Hassan, Soliman, Ashraf T., De Sanctis, Vincenzo, Yassin, Mohamed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207785/
https://www.ncbi.nlm.nih.gov/pubmed/34134694
http://dx.doi.org/10.1186/s12967-021-02931-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207785/
https://www.ncbi.nlm.nih.gov/pubmed/34134694
http://dx.doi.org/10.1186/s12967-021-02931-1

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