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A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies
HbQ India is a rare α-chain structural hemoglobinopathy usually asymptomatic and presents in the heterozygous form or co-inherited with β-thalassemia trait. Herein, we are reporting the third case of novel association of HbQ India with HbS trait hemoglobinopathy in a 30-year-old young male presented...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8723905/ https://www.ncbi.nlm.nih.gov/pubmed/35005433 http://dx.doi.org/10.1007/s42399-021-01103-y |