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Article

βS globin gene haplotype and the stroke risk among Egyptian children with sickle cell disease.

Hematology (Amsterdam, Netherlands) - 1 Jul 2018

Abou-Elew Heba H, Youssry Ilham, Hefny Shireen, Hashem Rania H, Fouad Nevine, Zayed Rania A

Abstract excerpt

BACKGROUND AND AIM OF WORK: Sickle cell disease (SCD) is an inherited disease of the beta globin gene. The βS globin gene haplotypes are Senegal, Benin, Bantu, Cameroon, Arab-Indian and atypical haplotypes. In SCD, stroke is a life-threatening event in both adults and children. In light of paucity of studies on βS globin gene haplotypes in Egypt, we aimed to determine βS globin gene haplotypes in children with...

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Source

Identifiers

PMID: 29157167
DOI: 10.1080/10245332.2017.1403736

Genes

SCD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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