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Incidental Identification of Possible Delta-Beta Thalassemia Trait in a Family: A Rare Cause of Elevated Hb F.
Delta-Beta thalassaemia is an unusual variant of thalassaemia with elevated level of foetal haemoglobin (HbF). The clinical presentation of delta-beta thalassaemia is mild in both heterozygote and homozygote cases. We hereby describe a rare cause of elevated Hb F in a father and his two daughters. A...
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| Publicat a: | J Clin Diagn Res |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
JCDR Research and Publications (P) Limited
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4843246/ https://ncbi.nlm.nih.gov/pubmed/27134860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2016/16352.7409 |
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