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Article

Sickle Cell Disease in Jordan: The Experience of a Major Referral Center.

Medical archives (Sarajevo, Bosnia and Herzegovina) - 1 Feb 2021

Oudat Raida I, Abualruz Heba S, Al-Shiek Nazih Kh Abu, Al-Mashaqba Eman A, Al-Hiari Rawan A, Alsoukhni Hala A, Hammad Ma'mon A Abu

Abstract excerpt

INTRODUCTION: Sickle cell disorders are the most frequently encountered hemoglobin variants in Jordan. Both alpha and beta thalassemias are also prevalent in this population. However, studies on the interaction between these hemoglobin disorders are lacking. AIM: To determine the genotypes responsible for Sickle cell disease in Jordan, by retrospectively reviewing the data from a major referral center in the...

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Identifiers

PMID: 34012195
DOI: 10.5455/medarh.2021.75.27-30
PMCID: PMC8116085

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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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