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Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

From: Diagnostic value of fetal hemoglobin Bart’s for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy

Fig. 3

A Pedigree analysis of a family in which the fetus was a double heterozygote for Hb Queens Park/Hb E. The father was a carrier of α0-thalassemia (SEA deletion) and the mother was a patient with Hb H-Queens Park disease with Hb E heterozygote (the Hb Queens Park-AEBart’s). Hematological parameters of all members are listed. B Pedigree analysis of a family in which the fetus was double heterozygote for Hb Amsterdam A1/Hb E. No blood specimen of the father was available. Hematological parameters of the mother and the fetus are listed

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172