目的：探讨骨髓铁染对缺铁性贫血和慢性疾病性贫血的鉴别诊断价值。
Objective To explore the value of differential diagnosis on iron-deficiency anemia and chromic diseases anemia with marrow iron-stain.
结论：骨髓铁染色是鉴别诊断缺铁性血和慢性疾病性贫血简单易行的方法。
Conclusion Marrow iron-stain is one of simple and safe methods of differential diagnosis on iron-deficiency anemia and chromic diseases anemia.
慢性疾病性贫血是一类以血清铁低、总铁结合力低、贮存铁增加为特征的贫血。
Anemia of chronic disease is an anemia characterized by reduced serum iron concentrations, total iron binding capacity, whereas iron stores are increased.
不同慢性系统疾病性贫血男、女患者之间RDW值差异均无显著性（P>0.05）。
No significant differences could be found in the RDW values between male and female patients with the three different kinds of anemia(P>0.05).
方法：选取缺铁性贫血、慢性疾病性贫血的骨髓片行染色检查，显微镜下检测细胞内外铁。
Method Some patients with iron-deficiency anemia and chronic disease anemia were selected and the level of iron in cells and out of cells by marrow iron-stain detected.
对于骨髓疾病相关性贫血。治疗方法很多，从简单的药物到化疗到骨髓移植。
Anemias associated with bone marrow disease. Treatment of these various diseases can range from simple medication to chemotherapy to bone marrow transplantation.
如西非人以及他们的后代易患一种叫做镰状细胞性贫血的疾病，这种病在西非之外几乎都没人听说过。
West Africans, and people of West African descent, are susceptible to a disease called sickle-cell anaemia that is virtually unknown elsewhere.
对于骨髓疾病相关性贫血。
溶血性尿毒综合征是一种危及生命的疾病，其特征是急性肾功能衰竭(尿毒症)、溶血性贫血以及低血小板(血小板减少症)。
Haemolytic uraemic syndrome (HUS) is a life-threatening disease characterized by acute renal failure (uraemia), haemolytic anaemia, and a low platelet count (thrombocytopenia).
或检测血液细胞是否有镰状细胞性贫血，白血病或其他疾病的迹象。
Or blood cells may be examined for signs of sickle-cell anemia, leukemia, or other disorders.
镰状细胞性贫血是最流行的遗传性疾病之一，具有很高的发病率和死亡率。
Sickle-cell anemia is one of the most prevalent hereditary disorders with prominent morbidity and mortality.
本节内容适用于白血病，淋巴瘤，骨髓癌以及其它血液疾病，如遗传性贫血和再生障碍性贫血。
This section contains information that applies to leukemia, lymphoma , myeloma and other hematological conditions, such as hereditary anemias and aplastic anemia.
其它研究已经把维生素b 12缺乏与恶性贫血，心血管疾病，癌症和神经再生紊乱联系起来了。
Other studies have linked B12 deficiency with pernicious anemia, cardiovascular disease, cancer, and neurodegenerative disorders.
不过，CRISPR这种基因编辑技术可是货真价实的。它有可能在未来的某一天治愈细胞性贫血等与基因相关的疾病，种出更好的庄稼，或者带来大量可供移植的器官。
But CRISPR is very real, with the potential, one day, to cure genetically-linked diseases like sickle cell anemia, produce better crops, and create a huge supply of organs for transplant.
瘙痒也可能是肝病、肾功能衰竭、缺铁性贫血、甲状腺和甲状旁腺疾病的突出症状。
Liver disease, renal failure, iron deficiency, and thyroid or parathyroid disease are other systemic diseases in which pruritus may be prominent.
慢性再生障碍性贫血（CAA）是临床难治的血液疾病，其致病原因复杂，发病机制多样。
Chronic aplastic anemia (CAA), with complex causings of disease and multiple pathogenic mechanism, is a refractory blood disease.
研究发现，各型基因突变均可引起新生儿高胆红素血症、急性溶血性贫血等，也与病毒性肝炎、白血病、淋巴瘤等疾病的发生有一定关系。
Our Studies suggest that all the gene mutation may le AD to jaundice of the newborn, acute hemolytic anaemia, and have some relation to viral hepatitis, leukaemia, lymphoma.
铜含量也是威尔逊氏症病、小细胞低色素性贫血和由胶原蛋白合成减少引起骨髓疾病的关键诊断参数。
Levels of copper are key diagnostic indicator of diseases such as Wilsons disease, microcytic hypochromic anaemia and bone disease due to reduced collagen synthesis.
排除严重肝肾功能不全、营养不良、严重恶性疾病（如恶性肿瘤）、恶性贫血、糖尿病病人。
The following conditions were excluded: severe hepatic and renal dysfunction, malnutrition, malignant tumour, malignant anemia, diabetes.
镰状细胞性贫血和亨庭顿综合症就是这样的疾病，单个变异起了很大的作用。
Examples of so-called SNP diseases are sickle-cell anemia and Huntington's disease, where a single variant or mutation has a dramatic effect.
这个案件被170个人抱怨，他们的孩子，遭受血友病和血液疾病珠蛋白生成障碍性贫血的痛苦。
The case followed complaints by families of some 170 people, many of them children, suffering from haemophilia and the blood disease thalassemia.
美国患adpkd的人数超过囊性纤维化、肌营养不良、血友病、唐氏综合症、镰刀细胞性贫血数种疾病加起来的患者。
In the U. S., the number of individuals affected by ADPKD is greater than the number affected by cystic fibrosis, muscular dystrophy, hemophilia, Down's syndrome, and sickle cell anemia combined.
同样的精卵结合方式很可能应用于“移植前基因诊断”，给那些患有其他基因疾病的人，包括白血病和珠蛋白生成障碍性贫血患者带来希望。
The same ready acceptance is likely to apply to PGD, which offers hope to sufferers of other genetic disorders, including leukaemia4 and thalas-saemia.
同样的精卵结合方式很可能应用于“移植前基因诊断”，给那些患有其他基因疾病的人，包括白血病和珠蛋白生成障碍性贫血患者带来希望。
The same ready acceptance is likely to apply to PGD, which offers hope to sufferers of other genetic disorders, including leukaemia4 and thalas-saemia.
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