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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...

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Detalles Bibliográficos
Autores principales: Gupta, Rakesh K., Verma, Kartavya Kumar, Singh, Gurmeet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
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