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Research ArticleOriginal Article
Open Access

The accurate prediction of rare hemoglobin variants using a combination of high performance liquid chromatography, retention time and isoelectric focusing electrophoresis position

Mohamed S. Khalil, Adele T. Molyneux, Samy Marouf, Ghazy A. Eldamanhory, Anna H. Schuh, Shirley J. Henderson and John M. Old
Saudi Medical Journal September 2009, 30 (9) 1158-1164;
Mohamed S. Khalil
National Hemoglobinopathy Laboratory, Molecular Hematology, Churchill Hospital, Oxford, United Kingdom.
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Adele T. Molyneux
National Hemoglobinopathy Laboratory, Molecular Hematology, Churchill Hospital, Oxford, United Kingdom.
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Samy Marouf
National Hemoglobinopathy Laboratory, Molecular Hematology, Churchill Hospital, Oxford, United Kingdom.
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Ghazy A. Eldamanhory
National Hemoglobinopathy Laboratory, Molecular Hematology, Churchill Hospital, Oxford, United Kingdom.
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Anna H. Schuh
National Hemoglobinopathy Laboratory, Molecular Hematology, Churchill Hospital, Oxford, United Kingdom.
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Shirley J. Henderson
National Hemoglobinopathy Laboratory, Molecular Hematology, Churchill Hospital, Oxford, United Kingdom.
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John M. Old
National Hemoglobinopathy Laboratory, Molecular Hematology, Churchill Hospital, Oxford, United Kingdom.
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Abstract

OBJECTIVE: To investigate the predictive accuracy of using a combination of the high pressure liquid chromatography (HPLC) retention time and the relative isoelectric focusing (IEF) position to diagnose rare hemoglobin variants.

METHODS: A selected group of 40 patients with a rare beta-chain variant were assigned a presumed diagnosis following HPLC and IEF screening and then the variant identified in each case by DNA analysis. The study was conducted at the National Hemoglobinopathy Reference Laboratory, Oxford, United Kingdom, from August 2008 to October 2008.

RESULTS: Thirteen out of 14 different variants were predicted accurately in 39 (97.5%) cases, compared to only one each for HPLC and IEF when used individually. A novel amplification refractory mutation system-polymerase chain reaction test was developed for Hb J-Baltimore and used successfully, to provide a simple, rapid, and inexpensive diagnosis.

CONCLUSION: The use of both HPLC retention time and isoelectric focusing position provides an accurate presumed diagnosis of a rare hemoglobin variant in the majority of cases. Amplification refractory mutation system-polymerase chain reaction test can provide a simple, rapid and inexpensive molecular diagnostic method for rare beta-chain variants.

  • Copyright: © Saudi Medical Journal

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Saudi Medical Journal: 30 (9)
Saudi Medical Journal
Vol. 30, Issue 9
1 Sep 2009
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The accurate prediction of rare hemoglobin variants using a combination of high performance liquid chromatography, retention time and isoelectric focusing electrophoresis position
Mohamed S. Khalil, Adele T. Molyneux, Samy Marouf, Ghazy A. Eldamanhory, Anna H. Schuh, Shirley J. Henderson, John M. Old
Saudi Medical Journal Sep 2009, 30 (9) 1158-1164;

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The accurate prediction of rare hemoglobin variants using a combination of high performance liquid chromatography, retention time and isoelectric focusing electrophoresis position
Mohamed S. Khalil, Adele T. Molyneux, Samy Marouf, Ghazy A. Eldamanhory, Anna H. Schuh, Shirley J. Henderson, John M. Old
Saudi Medical Journal Sep 2009, 30 (9) 1158-1164;
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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