无症状的
血红蛋白
小细胞性贫血
复合杂合度
贫血
胎儿血红蛋白
医学
杂合子丢失
等位基因
珠蛋白
内科学
胃肠病学
遗传学
生物
胎儿
怀孕
基因
作者
Dafna Brik Simon,Dvora Filon,Vardiella Meiner,Tanya Krasnov,Sharon Noy‐Lotan,Orly Dgany,Oded Gilad,Tracie Goldberg,Shai Izraeli,Joanne Yacobovich,Hannah Tamary,Orna Steinberg‐Shemer
摘要
Hemoglobin City of Hope (Hb-COH), NC_000011.9(NM_000518.5):c.208G > A; NP_000509.1:p.(Gly70Ser), has rarely been described. The presentation ranges from asymptomatic heterozygosity to significant anemia in patients carrying an additional pathogenic variant in β-globin. To elucidate the clinical spectrum of Hb-COH, we analyzed 31 individuals carrying the variant, including, for the first time, homozygous individuals. Seven patients who were compound heterozygous for Hb-COH and an additional variant in β-globin, presented with mild-to-severe microcytic anemia and elevated hemoglobin-A2. Three (43%) of these also had elevated fetal hemoglobin, but none required blood transfusions. Seven patients coinherited Hb-COH with an -α
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