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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Autores principales: Gupta, Rakesh K., Verma, Kartavya Kumar, Singh, Gurmeet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Case Report
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
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author Gupta, Rakesh K.
Verma, Kartavya Kumar
Singh, Gurmeet
author_facet Gupta, Rakesh K.
Verma, Kartavya Kumar
Singh, Gurmeet
author_sort Gupta, Rakesh K.
collection PubMed
description 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 with chief complaints of yellowish discoloration of sclera since 5 years with raised serum bilirubin levels along with pedigree analysis of the family.
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spelling pubmed-87239052022-01-04 A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies Gupta, Rakesh K. Verma, Kartavya Kumar Singh, Gurmeet SN Compr Clin Med Case Report 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 with chief complaints of yellowish discoloration of sclera since 5 years with raised serum bilirubin levels along with pedigree analysis of the family. Springer International Publishing 2022-01-04 2022 /pmc/articles/PMC8723905/ /pubmed/35005433 http://dx.doi.org/10.1007/s42399-021-01103-y Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Case Report
Gupta, Rakesh K.
Verma, Kartavya Kumar
Singh, Gurmeet
A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies
title A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies
title_full A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies
title_fullStr A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies
title_full_unstemmed A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies
title_short A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies
title_sort novel association of hbq india trait with sickle cell anemia: a new insight in hemoglobinopathies
topic Case Report
url 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
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