首次报告毛细管电泳中的 Youngstown 血红蛋白以及与 Rush 血红蛋白重叠的血红蛋白分析结果。

IF 1.2 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hemoglobin Pub Date : 2024-07-01 Epub Date: 2024-09-03 DOI:10.1080/03630269.2024.2398236
Kim Yan Poh, Ping Chong Bee
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引用次数: 0

摘要

Youngstown 血红蛋白[HBB:c.305A > C]是一种罕见的不稳定血红蛋白,由 Beta 球蛋白链第 101 个密码子上的谷氨酸被丙氨酸取代引起。在杂合状态下,它会导致溶血性贫血。本病例是一名六岁的中国-爪哇女孩,她患有杂合子 Youngstown 血红蛋白,临床特征为慢性溶血和铁超载。在高效液相色谱(HPLC)上,Hb Youngstown 出现在接近 4.6 分钟的 S 窗口,在碱性凝胶电泳上可形成混合四聚体,表现为两条不同的条带,分别位于 A 的阴极和 F 的附近。这种杂合型血红蛋白 Youngstown 的临床表现和血红蛋白分析结果与杂合型血红蛋白 Rush 重叠。只有通过β球蛋白基因测序或完整的质谱分析才能在分子水平上将它们区分开来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First Report of Hb Youngstown in Capillary Electrophoresis and Overlapping Hb Analysis Findings with Hb Rush.

Hb Youngstown [HBB:c.305A > C] is a rare unstable hemoglobin caused by the substitution of glutamic acid with alanine at codon 101 of the Beta globin chain. It causes hemolytic anemia in the heterozygous state. This is a case of a six-year-old Chinese-Javanese girl with heterozygous Hb Youngstown and clinical features of chronic hemolysis and iron overload. Hb Youngstown appears at the S window near to 4.6 minutes on high-performance liquid chromatography (HPLC) and can form a hybrid tetramer on alkaline gel electrophoresis seen as two distinct bands cathodal to A and close to F. For the first time, Hb Youngstown is captured with capillary electrophoresis (CE) and shown to be eluted at zone 8. Clinical presentation and Hb analysis results of this heterozygous Hb Youngstown overlap with heterozygous Hb Rush. They can only be differentiated at molecular level by Beta globin gene sequencing or intact mass spectrometry.

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来源期刊
Hemoglobin
Hemoglobin 医学-生化与分子生物学
CiteScore
1.70
自引率
10.00%
发文量
59
审稿时长
3 months
期刊介绍: Hemoglobin is a journal in the English language for the communication of research and information concerning hemoglobin in humans and other species. Hemoglobin publishes articles, reviews, points of view The journal covers topics such as: structure, function, genetics and evolution of hemoglobins biochemical and biophysical properties of hemoglobin molecules characterization of hemoglobin disorders (variants and thalassemias), consequences and treatment of hemoglobin disorders epidemiology and prevention of hemoglobin disorders (neo-natal and adult screening) modulating factors methodology used for diagnosis of hemoglobin disorders
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