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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 1
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Original Article

Hb Den Haag [β45(CD4)Phe→Tyr]. A New Hemoglobin Variant Observed During Early Pregnancy Diagnostics

Judith O. Kaufmann The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Cornelis L. Harteveld The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Margreet Bakker-Verweij The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Sandra G.J. Arkesteijn The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Peter van Delft The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Hans Haak Department of Hematology and Clinical Chemistry, HAGA City Hospital, The Hague, The Netherlands
,
Pierre W. Wijermans Department of Hematology and Clinical Chemistry, HAGA City Hospital, The Hague, The Netherlands
,
Jean-Louis Kerkhoffs Department of Hematology and Clinical Chemistry, HAGA City Hospital, The Hague, The Netherlands
&
Piero C. Giordano The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The NetherlandsCorrespondence[email protected]
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Pages 37-44 | Received 28 Apr 2009, Accepted 29 Sep 2009, Published online: 01 Feb 2010

REFERENCES

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  • Giordano PC, Plancke A, Van Meir CA, Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot study. Prenat Diagn. 2006;26(8):719–724.
  • Giordano PC, Addo-Daaku A, Sander MJ, The rare Hb Showa-Yakushiji [β110(G12)Leu→Pro, CTG→CCG] in combination with an α gene triplication found in a Dutch patient during her first pregnancy examination. Hemoglobin. 2007;31(2):167–171.
  • Van Delft P, Lenters E, Bakker-Verweij M, de Korte M, Harteveld CL, Giordano PC. Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations. Int J Lab Hematol. 2009;31(5):484–895.
  • Giordano PC, Maatman RG, Niessen RW, van Delft P, Harteveld CL. β Thalassemia IVS-I-5 (G→C) heterozygosity masked by the presence of Hb J-Meerut in a Dutch-Indian patient. Haematologica. 2006;91(12 Suppl):ECR56.
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  • Yeager AM, Zinkham WH, Jue DL, Hemoglobin Cheverly: an unstable hemoglobin associated with chronic mild anemia. Pediatr Res. 1983;17(6):503–507.
  • Vassilopoulos G, Papassotiriou I, Voskaridou E, Hb Arta [β45(CD4)Phe→Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with β-thalassaemia. Br J Haematol. 1995;91(3):595–601.
  • Marden MC, Dewilde S, Kiger L, Exploiting a list of protein sequences. Gene. 2007;398(1–2):35–41.
  • Winterbourn CC. Oxidative denaturation in congenital hemolytic anemias: the unstable hemoglobins. Semin Hematol. 1990;27(1):41–50.

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