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首页> 外文期刊>Hemoglobin: International Journal for Hemoglobin Research >The first case of Hb G-Honolulu [α30(B11)Glu→Gln (GAG>CAG); HBA2:c.91G>A] observed in association with Hb S [β6(A3)Glu→Val, GAG>GTG] in a healthy Italian child
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The first case of Hb G-Honolulu [α30(B11)Glu→Gln (GAG>CAG); HBA2:c.91G>A] observed in association with Hb S [β6(A3)Glu→Val, GAG>GTG] in a healthy Italian child

机译:Hb G-檀香山[α30(B11)Glu→Gln(GAG> CAG);在健康的意大利儿童中观察到HBA2:c.91G> A]与Hb S [β6(A3)Glu→Val,GAG> GTG]相关联

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摘要

We report the first observation of Hb G-Honolulu [α30(B11) Glu→Gln (GAGCAG); HBA2:c.91GA] in a Caucasian family and the first case of this variant to be found in association with Hb S [β6(A3) Glu→Val, GAGGTG]. The proband was a healthy 4-year-old Italian boy. His chromatographic hemoglobin (Hb) pattern showed an abnormal peak having the typical retention time of Hb S (25.6% ), a second abnormal peak eluted soon after (13.6%) and a third minor peak eluted at the end of the run (6.5%). Identification of Hb variants were performed by peptide mapping using liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS). Two abnormal peptides at m/z 765.1 and 922 were found, corresponding to the αT-4 and βT-1 peptides characteristic for Hb G-Honolulu and Hb S, respectively. The third minor abnormal peak presumably corresponded to the hybrid molecule (α G-Honolulu/β S). The concomitant presence of Hb G-Honolulu and Hb S does not seem to produce any relevant clinical manifestation.
机译:我们报告了Hb G-檀香山[α30(B11)Glu→Gln(GAG> CAG);白人家庭中的HBA2:c.91G> A],并且该变体的第一个病例与Hb S [β6(A3)Glu→Val,GAG> GTG]相关。先证者是一个健康的4岁意大利男孩。他的色谱血红蛋白(Hb)图谱显示一个具有典型Hb S保留时间的异常峰(25.6%),第二个异常峰在洗脱后不久被洗脱(13.6%),第三个次要峰在运行结束时被洗脱(6.5%) )。通过使用液相色谱-电喷雾电离串联质谱法(LC-ESI-MS / MS)进行肽图分析来鉴定Hb变体。发现了m / z 765.1和922处的两个异常肽,分别对应于Hb G-檀香山和Hb S的特征性αT-4和βT-1肽。第三个次要异常峰大概对应于杂合分子(αG-檀香山/βS)。 Hb G-檀香山和Hb S的并存似乎没有产生任何相关的临床表现。

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