A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease

Generally, within the ABO blood group system, the AB group is subdivided into two subtypes, A(1)B and A(2)B, with the A(2)B subtype considered to be the rarest and the A(1)B subtype the most common. Given that the A(2)B subtype is the rarest one, its presence is associated with many challenges. In t...

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Autores principales: Busaleh, Fadi, Bu-Izran, Dunya, Alhajji, Zainab, Qahtan, Rawya, Alnaaim, Abdulatif, Alnofaily, Haider, Almohammed, Salah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799867/
https://www.ncbi.nlm.nih.gov/pubmed/35141073
http://dx.doi.org/10.7759/cureus.20815
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author Busaleh, Fadi
Bu-Izran, Dunya
Alhajji, Zainab
Qahtan, Rawya
Alnaaim, Abdulatif
Alnofaily, Haider
Almohammed, Salah
author_facet Busaleh, Fadi
Bu-Izran, Dunya
Alhajji, Zainab
Qahtan, Rawya
Alnaaim, Abdulatif
Alnofaily, Haider
Almohammed, Salah
author_sort Busaleh, Fadi
collection PubMed
description Generally, within the ABO blood group system, the AB group is subdivided into two subtypes, A(1)B and A(2)B, with the A(2)B subtype considered to be the rarest and the A(1)B subtype the most common. Given that the A(2)B subtype is the rarest one, its presence is associated with many challenges. In this report, we present the case of a child with a chronic hemolytic disease with the A(2)B blood group but without anti-A1 lectin antibodies, as well as the challenges encountered.
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spelling pubmed-87998672022-02-08 A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease Busaleh, Fadi Bu-Izran, Dunya Alhajji, Zainab Qahtan, Rawya Alnaaim, Abdulatif Alnofaily, Haider Almohammed, Salah Cureus Pediatrics Generally, within the ABO blood group system, the AB group is subdivided into two subtypes, A(1)B and A(2)B, with the A(2)B subtype considered to be the rarest and the A(1)B subtype the most common. Given that the A(2)B subtype is the rarest one, its presence is associated with many challenges. In this report, we present the case of a child with a chronic hemolytic disease with the A(2)B blood group but without anti-A1 lectin antibodies, as well as the challenges encountered. Cureus 2021-12-29 /pmc/articles/PMC8799867/ /pubmed/35141073 http://dx.doi.org/10.7759/cureus.20815 Text en Copyright © 2021, Busaleh et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatrics
Busaleh, Fadi
Bu-Izran, Dunya
Alhajji, Zainab
Qahtan, Rawya
Alnaaim, Abdulatif
Alnofaily, Haider
Almohammed, Salah
A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease
title A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease
title_full A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease
title_fullStr A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease
title_full_unstemmed A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease
title_short A2B Blood Group Without Anti-A1 Lectin Antibodies in a Child With an Enzymopathy Hemolytic Disease
title_sort a2b blood group without anti-a1 lectin antibodies in a child with an enzymopathy hemolytic disease
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799867/
https://www.ncbi.nlm.nih.gov/pubmed/35141073
http://dx.doi.org/10.7759/cureus.20815
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