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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

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. 2

Pedigree analysis of a family in which fetal blood analysis identified that the fetus was a compound heterozygote for Hb CS/Hb Pakse’ in association with heterozygous Hb E. Due to the lack of specimens of the parents, their exact thalassemia genotypes could not be defined. Hematological parameters of the fetus are listed and Hb analysis profiles using capillary electrophoresis are shown with Hb Bart’s 13.6%

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172