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HbH disease is characterised by a moderate anaemia (Hb typically ~80g/L, but can range from 60-100g/L). Haemolytic episodes are triggered by infections, especially parvovirus B19 …

2009年1月1日 · Hemoglobin H (Hb H) disease is the most severe non-fatal form of α-thalassemia syndrome, mostly caused by molecular defects of the α-globin genes in which α-globin …

Hemoglobin H disease is named for the abnormal hemoglobin H (created by the remaining beta globin) that destroys red blood cells. Alpha-thalassemia is an inherited blood disorder that …

Hemoglobin H disease (HbH) is a form of alpha thalassemia in which moderately severe anemia develops due to reduced formation of alpha globin chains. In this condition, as in the other …

α地中海贫血在临床上一般分为四种类型：静止型携带者、α地中海贫血特征、HbH病和Hb Bart胎儿水肿综合征。 静止型携带者及α地中海贫血特征者无任何症状及特征。 HbH患者出生时与正 …

血红蛋白 病（hemoglobinopathy）是由于 血红蛋白分子 结构异常 （异常血红蛋白病），或 珠蛋白 肽链 合成速率异常（珠蛋白生成障碍性贫血，又称 海洋性贫血）所引起的一组 遗传性 血 …

2021年1月28日 · Hematological analysis revealed a severe hypochromic, microcytic anemia, and HbH inclusions in 30.7% of cells, but no evidence of iron overload (Figure 2A-C; supplemental …

2018年9月6日 · 珠蛋白生成障碍性贫血（thalassemia），即地中海贫血（简称地贫），是由于基因缺陷导致血红蛋白中一种或一种以上珠蛋白肽链合成缺如或不足所发生的遗传性溶血性贫血 …

海洋性貧血即所謂地中海型貧血，是血紅素（Hemoglobin）的血紅蛋白鏈（Globin chain）合成發生問題，以致該種血紅蛋白鏈的合成量降低或完全無法製造，而使得紅血球的體積較小（即小 …