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Article

Molecular Understanding of Severe Cases of β-Thalassemia in the Nablus Region, West Bank, Palestine.

Hemoglobin - 1 Mar 2020

Samha Leen, Sirdah Mahmoud M, Reading N Scott, Karmi Bashar, Agarwal Archana M

Abstract excerpt

Hemoglobinopathies are common inherited monogenic diseases that are likely to remain a serious regional health problem where thalassemias and sickle cell disease are prevalent. In regions where recessive alleles for hemoglobinopathy disorders are present with high consanguinity rates, such as in Palestine, coinheritance of two different genetic defects becomes anticipated and prevalent. In this report, we...

Topics

Adolescent
Adult
Aged
Arabs
Child
Female
Genetic Predisposition to Disease
Genetic Variation
Hemoglobins, Abnormal
Humans
Male
Middle Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Middle East

Severity of Illness Index

Young Adult

beta-Thalassemia

Source

Identifiers

PMID: 32420772
DOI: 10.1080/03630269.2020.1763398

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-32420772-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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