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Unexpected discovery of hemoglobinopathy C/β° thalassemia
High performance liquid chromatography (HPLC) is the current method of choice for the detection of hemoglobinopathies and the quantification of A2 and fetal hemoglobin. We are describing a case where a double heterozygosity C/beta‐thalassemia was fortuitously identified, during assaying HBA1c, by HP...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6230608/ https://www.ncbi.nlm.nih.gov/pubmed/30455903 http://dx.doi.org/10.1002/ccr3.1815 |
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| author | Bouyarmane, Wafaa Uwingabiye, Jean Biaz, Asmaa Rachid, Achraf Mechal, Youness Dami, Abdellah Bouhsain, Sanae Ouzzif, Zhor El Machtani Idrissi, Samira |
| author_facet | Bouyarmane, Wafaa Uwingabiye, Jean Biaz, Asmaa Rachid, Achraf Mechal, Youness Dami, Abdellah Bouhsain, Sanae Ouzzif, Zhor El Machtani Idrissi, Samira |
| author_sort | Bouyarmane, Wafaa |
| collection | PubMed |
| description | High performance liquid chromatography (HPLC) is the current method of choice for the detection of hemoglobinopathies and the quantification of A2 and fetal hemoglobin. We are describing a case where a double heterozygosity C/beta‐thalassemia was fortuitously identified, during assaying HBA1c, by HPLC. |
| format | Online Article Text |
| id | pubmed-6230608 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2018 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-62306082018-11-19 Unexpected discovery of hemoglobinopathy C/β° thalassemia Bouyarmane, Wafaa Uwingabiye, Jean Biaz, Asmaa Rachid, Achraf Mechal, Youness Dami, Abdellah Bouhsain, Sanae Ouzzif, Zhor El Machtani Idrissi, Samira Clin Case Rep Case Reports High performance liquid chromatography (HPLC) is the current method of choice for the detection of hemoglobinopathies and the quantification of A2 and fetal hemoglobin. We are describing a case where a double heterozygosity C/beta‐thalassemia was fortuitously identified, during assaying HBA1c, by HPLC. John Wiley and Sons Inc. 2018-09-21 /pmc/articles/PMC6230608/ /pubmed/30455903 http://dx.doi.org/10.1002/ccr3.1815 Text en © 2018 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://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 Reports Bouyarmane, Wafaa Uwingabiye, Jean Biaz, Asmaa Rachid, Achraf Mechal, Youness Dami, Abdellah Bouhsain, Sanae Ouzzif, Zhor El Machtani Idrissi, Samira Unexpected discovery of hemoglobinopathy C/β° thalassemia |
| title | Unexpected discovery of hemoglobinopathy C/β° thalassemia |
| title_full | Unexpected discovery of hemoglobinopathy C/β° thalassemia |
| title_fullStr | Unexpected discovery of hemoglobinopathy C/β° thalassemia |
| title_full_unstemmed | Unexpected discovery of hemoglobinopathy C/β° thalassemia |
| title_short | Unexpected discovery of hemoglobinopathy C/β° thalassemia |
| title_sort | unexpected discovery of hemoglobinopathy c/β° thalassemia |
| topic | Case Reports |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6230608/ https://www.ncbi.nlm.nih.gov/pubmed/30455903 http://dx.doi.org/10.1002/ccr3.1815 |
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