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Fig. 6 | Orphanet Journal of Rare Diseases

Fig. 6

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. 6

Pedigree analysis of a family in which fetal blood analysis identified that the fetus was suffered from the Hb H disease with Hb Quong Sze (--SEA/αQZα). In contrast, the father was a carrier of α0-thalassemia (SEA deletion) and the mother was a carrier of Hb Quong Sze. Hematological parameters of all members are listed with the fetal Hb Bart’s of 33.7%. na not available

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172