Overview
Delta thalassaemia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "delta-Thalassemias" from the MEDLINE/PubMed database.
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Homozygous Delta-Beta Thalassaemia With Alpha Thalassaemia and Erythrocytosis- a Rare Case Report.
[object Object], [object Object], [object Object] et al. · Br J Biomed Sci · 2024
δβ-Thalassemia and α-Triplication: Is Genetic Retesting Worthwhile in Case of Non-Coherent Phenotype?
[object Object], [object Object], [object Object] et al. · Hemoglobin · 2024
PMID: 39402933Case Report
Hb SKMC and an unprecedented γδβ-thalassemia: first report from Iraq.
[object Object], [object Object], [object Object] et al. · Hematology · 2024
PMID: 39252479Case Report
Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.
[object Object], [object Object], [object Object] et al. · Int J Lab Hematol · 2014
PMID: 23621512Review
Molecular Characterization of δβ Thalassemia/Hereditary Persistence of Fetal Hemoglobin and Its Correlation With Clinical and Hematological Profile; a Single Center Study in North India.
[object Object], [object Object], [object Object] et al. · Int J Lab Hematol · 2025
PMID: 39731309Other
Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)-Thalassemia among Tunisian family.
[object Object], [object Object], [object Object] et al. · Ann Clin Biochem · 2023
PMID: 36214153Other
False positive Hb Bart's immunochromatographic strip test for alpha thalassaemia in delta-beta thalassaemia carriers.
[object Object], [object Object], [object Object] et al. · Int J Lab Hematol · 2023
PMID: 37317650Other
Mutational spectrum of HBD gene in the Chinese population: Description of 36 mutations including 11 novel variants.
[object Object], [object Object], [object Object] et al. · Int J Lab Hematol · 2023
PMID: 37605839Other
Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.
[object Object], [object Object], [object Object] et al. · Mol Biol Rep · 2021
PMID: 34341901Other
Search all PubMed articles for Delta thalassaemia
Research data from MEDLINE/PubMed
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased haemoglobin
HP:0001903
Imbalanced hemoglobin synthesis
HP:0005560
Related Conditions
Quick Facts
- SNOMED CT
- 16427007
- UMLS CUI
- C0271990
- Fully Specified Name
- Delta thalassemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 2
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.