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A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report
We present these two cases to emphasize the necessity of critical thinking and high suspicion of the disease (Rogers syndrome) to avoid potentially fatal situations due to its rarity and the importance of early treatment.
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114085/ https://www.ncbi.nlm.nih.gov/pubmed/37091967 http://dx.doi.org/10.1002/ccr3.7192 |
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author | Deeb, Yara Martini, Nafiza Ahmad, Yara Ahmad Alkosti, Marwa Hamdan, Othman |
author_facet | Deeb, Yara Martini, Nafiza Ahmad, Yara Ahmad Alkosti, Marwa Hamdan, Othman |
author_sort | Deeb, Yara |
collection | PubMed |
description | We present these two cases to emphasize the necessity of critical thinking and high suspicion of the disease (Rogers syndrome) to avoid potentially fatal situations due to its rarity and the importance of early treatment. |
format | Online Article Text |
id | pubmed-10114085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101140852023-04-20 A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report Deeb, Yara Martini, Nafiza Ahmad, Yara Ahmad Alkosti, Marwa Hamdan, Othman Clin Case Rep Case Report We present these two cases to emphasize the necessity of critical thinking and high suspicion of the disease (Rogers syndrome) to avoid potentially fatal situations due to its rarity and the importance of early treatment. John Wiley and Sons Inc. 2023-04-19 /pmc/articles/PMC10114085/ /pubmed/37091967 http://dx.doi.org/10.1002/ccr3.7192 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Deeb, Yara Martini, Nafiza Ahmad, Yara Ahmad Alkosti, Marwa Hamdan, Othman A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report |
title | A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report |
title_full | A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report |
title_fullStr | A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report |
title_full_unstemmed | A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report |
title_short | A challenging diagnosis for thiamine transporter deficiency anemia (Rogers syndrome) in two young siblings: A rare case report |
title_sort | challenging diagnosis for thiamine transporter deficiency anemia (rogers syndrome) in two young siblings: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114085/ https://www.ncbi.nlm.nih.gov/pubmed/37091967 http://dx.doi.org/10.1002/ccr3.7192 |
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