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Article

The Sickle β-Thalassemia Phenotype.

Journal of pediatric hematology/oncology - 1 Jul 2017

Adekile Adekunle D, Akbulut Nagihan, Azab Asmaa F, Al-Sharida Sundus, Thomas Diana

Abstract excerpt

Sβ-thalassemia (Sβ-thal) is common among Gulf Arab patients with sickle cell disease, but the phenotype of this group had not been well-documented. We have studied a group of Kuwaiti patients and compared the phenotype in the homozygotes (SS) and Sβ-thal patients. Complete blood count, hemoglobin quantitation, serum bilirubin, and lactate dehydrogenase were determined with standard techniques. The patients were...

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Source

Identifiers

PMID: 28060121
DOI: 10.1097/MPH.0000000000000747

Genes

HBG2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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