网络甲型海洋性贫血 网络释义 1. 甲型海洋性贫血 甲型海洋性贫血(HbH disease)L72-048 Hb eletrophoresis Electrophoresis 海洋性贫血与异常血色素 L72-384 Hb A2 quantitation www1.cgmh.org.tw|基于 1 个网页
(1992) HbH disease in Sardinia: molecular, hematological and clinical aspects. Acta Haematologica, 88, 1-6.Galanello R, Aru B, Dessi C, Addis M, Paglietti E, Melis MA, et al. Hb H disease in Sardinia: molecular, hema- tological and clinical aspects. Acta Haematol 1992;88:1-6....
HBH病,全称为α0型地中海贫血(Hemoglobin H disease),是一种遗传性血红蛋白病。该疾病主要由α地中海贫血基因的突变引起,导致体内红细胞中的血红蛋白H(HbH)水平升高。本文将对HBH病基因型进行探讨,以及该病对患者的影响和治疗方法。 HBH病基因型通常指的是携带α地中海贫血基因的个体。正常情况下,人体内有四个α...
关键词:地中海贫血;HbH 病;突变;家系;基因诊断 Hemoglobin H disease with a rare α-thalassemia gene mutation (--SEA/α*92A>Gα): pedigree analysis and genetic diagnosis YAN Shanhuo1, LAO Kegan1, FU Kepeng1, GONG Feifei1, WEN Xiaojun2, ZHOU Wanjun2 1Qingzhou Maternal and Child Healthcare...
百度试题 结果1 题目HbH病(HbH disease)的基因型为A.--/--B. -1α-C.--/αα或-a/-αD.-a/aaE.aa/aa 相关知识点: 试题来源: 解析 B
Conclusion For the patients with low MCV and without HbH disease or with normal HbA2,α and β globin geneanalysis is necessary.〔Key words〕 Thalassemia;HbH disease;β-thalassemia;Gene diagnosis血红蛋白 H 病(HbH 病)是一种中间型 α-地中海贫血,从分子水平上可分为缺失型与非缺失型两类〔1〕 ...
关键词:HbQ-Thailand;血红蛋白H;α地中海贫血;产前诊断中图分类号 :R556.71 文献标识码 :A 文章编号 :1006-9534(2016)02-0012-02Molecular and prenatal diagnosis of hemoglobin H disease combining hemoglobin Q-Thailand. WANG Ji-cheng,QIN Dan-qing,DU Li,YUAN Teng-long,LUO Ming-yong*. (Guangdong ...
Summary. Globin gene mapping in 16 Greek individuals with HbH disease and their parents has demonstrated the occurrence of several HbH genotypes brought about by the interaction of two α+-thalassaemia and two α+-thalassaemia haplotypes. Eight of the 16 patients had the genotype Med/ -α3.7, ...
【关键词】 α 地中海贫血 ; 突变 ; 基因型 ; 表型Clinical phenotype genotype correlation in children with hemoglobin H disease in Zhuhai area of China ZHOU Yu2qiu , XIAO Qi2zhi , HUANG Li2juan , XIAO Ge2fei , LI Wen2dian , ZHU Lan2fang , CHEN Zi2xia ,ZHANG Yu2mei1 Zhuhai ...
一种罕见α-地贫基因突变HbH病(--SEA/α*92A>Gα)的家系分析与基因诊断 颜善活,劳可干,符可鹏,龚菲菲,温晓君,周万军 Hemoglobin H disease with a rare α-thalassemia gene mutation (--SEA/α*92A>Gα): pedigree analysis and genetic diagnosis 南方医科大学学报 . 2016, (09): 1295 ....