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An Unusual Case of Hemoglobin Bart's Hydrops Fetalis

Published online by Cambridge University Press:  01 August 2014

I. Halbrecht  and
F. Shabtai
I. Halbrecht*
Affiliation:
Research Institute of Human Reproduction and Fetal Development, Tel Aviv University Medical School, and Hasharon Hospital, Petah Tikva, Israel
F. Shabtai
Affiliation:
Research Institute of Human Reproduction and Fetal Development, Tel Aviv University Medical School, and Hasharon Hospital, Petah Tikva, Israel
*
Hasharon Hospital, Petah Tikva, Israel

Abstract

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A baby with alpha-chain thalassemia hydrops fetalis was born to an Iraqian Jewish couple of Iraqi-Kurdish extraction. Hemoglobin Bart's constituted only 40% of the total hemoglobin, much less than usually found in alpha-thalassemia hydrops fetalis.

That this is a particular expression of hemoglobin H disease is considered. The likelihood of two alpha-chain loci, rather than one alpha-chain locus, in this family, is also discussed.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 24 , Issue 1-2 , January 1975 , pp. 97 - 103
Copyright
Copyright © The International Society for Twin Studies 1975

References

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