白血红蛋白和β地中海贫血特征 - 通过序列分析和 MLPA 对 HBB 基因进行产前检测:病例报告

Saswati Mukhopadhyay
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引用次数: 0

摘要

勒波尔血红蛋白是一种由δ和β球蛋白链融合而成的融合球蛋白。这是一种缺失性血红蛋白病。在同基因型中,它与输血依赖型重型β地中海贫血相似,而在杂合子型中,它会导致轻度小红细胞低色素性贫血。在本病例报告中,这对夫妇患有杂合子莱波氏血红蛋白和杂合子β-地中海贫血症,妊娠期为 15 周。通过羊膜腔穿刺术进行产前检测,并通过测序和 MLPA 对胎儿进行 HBB 基因分析,以检测父母体内存在的不同类型的突变。本病例报告揭示了在进行桑格测序的同时进行 MLPA 检测 HBB 基因所有类型突变的重要性。
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Haemoglobin lepore and beta thalassaemia traits – Prenatal testing by both sequence analysis and MLPA for HBB gene: A case report
Hb Lepore is a fusion globin protein made of fused chains of delta and beta globin. It is a deletion haemoglobinopathy. In homozygote form, it is similar to transfusion dependent beta thalassaemia major, and in the heterozygous form, it causes mild microcytic hypochromic anaemia. In this case report, the couple has heterozygous Hb Lepore and heterozygous beta thalassaemia, with a pregnancy of 15weeks gestation. Prenatal testing by amniocentesis and HBB gene analysis for the fetus was done by sequencing and MLPA to detect the different types of mutations present in the parents. This case report reveals the importance of MLPA to be done along with sanger sequencing, to detect all types of mutations in the HBB gene.
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