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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

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. 1

Pedigree analysis of a family in which the father was a double heterozygote for Hb E/Hb CS and the mother was a compound Hb CS/α+-thalassemia (3.7 kb deletion). Fetal blood analysis identified that the fetus was a homozygous Hb CS. Hematological parameters of the fetus are listed and Hb analysis profiles using capillary electrophoresis are shown with Hb Bart’s 9.0%

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172