贫血

This testing method can be used for detection of characterized point mutations in β-thalassemia, which is convenient, reliable and economical for prenatal gene diagnosis of β-thalassemia with a broad prospect in aristogenesis.

MASPCR技术适合于检测β-地中海贫血已知点突变类型，是一种简便、可靠、经济的产前基因诊断方法，具有广阔的优生科学应用前景。

Potassium cravings should be satisfied because they may lead to cardiovascular diseases, asthenia, or anemia.

钾的渴望应该是满意的，因为它们可能导致心血管疾病，虚弱，或贫血。

The most common adverse events were neutropenia (n = 33), fever (21), influenza-like symptoms (21), asthenia (18), and gastrointestinal events (14). Anemia was reported in 6 patients.

最常见的不良反应包括中性粒细胞减少（33例）、发热（21例）、流感样症状（21例）、乏力（18例）和胃肠道症状（14例）。6例患者报告贫血。

The laboratory findings of a typical CCML patient comprised of peripheral blood leukocytosis, basophilia and eosinophilia,myeloid differentiation in different stages, and increased megakaryocytes. The immunohistochemical features of the CCML consisted of highly positive MPO and CD68, significant lowering of neutrophil alkaline phosphatase, positive for Philadel- phia chromosome or chimeric BCR/ABL gene, etc. But in most cases of juvenile CCML, the Philadelphia chromosome could not be detected.

临床表现以乏力、低热、贫血、肝脾及淋巴结肿大为主要特点；典型儿童慢性髓细胞白血病的实验室特点有白细胞计数高、嗜酸和嗜碱性粒细胞增多、骨髓不同阶段髓细胞分化和巨核细胞增多；免疫组化提示CD68，髓过氧化物酶，中性粒细胞碱性磷酸酶积分明显减低，Ph染色体或BCR/ABL融合基因阳性，而幼年型CCML的Ph染色体常为阴性。

Results The positive rate of binucleated granulocytes was 0%in normal contrast group. It was 53.0%in acute myeloid leukemia, 46.2%in chronic myeloid leukemia, 41.7%in reactive granulocytosis, and 38.4%in myelodysplastic syndrome. they were significantly higher than 8.2%in common anemia, 12.5%in idiopathic thrombocytopenic purpura, and 0%in lymphocytic leukemia.

结果 双核粒细胞阳性率，27例正常对照组为0，急性髓细胞白血病53.0%(80/151)、慢性髓细胞白血病46.2%(18/39)、反应性粒细胞增多症41.7%(20/48)、骨髓增生异常综合征38.4%(33/86)，明显高于一般贫血8.2%(8/98)、特发性血小板减少症12.5%(4/32)和急性淋巴细胞白血病为0。

Onset is 3-10 days after exposure Symptoms Severe crampy pain, tenderness over the colon or liver, loose morning stools, recurrent diarrhea, loss of weight, fatigue, and sometimes anemia.

发病是3-10天曝光后，症状严重crampy疼痛，压痛，在结肠或肝脏，松散上午凳子，经常性腹泻，体重下降，疲劳，有时贫血。

Hemoglobin values were determined by cyanmethemoglobin method according to the WHO1972 diagnostic criteria for anemia.

采用氰化高铁法测定血红蛋白值，诊断按WHO 1972年贫血筛查标准。

Objective To study the clinical, hematological and cytogenetical characteristics in Fanconi anemia.

目的研究范可尼贫血的临床学、血液学和细胞遗传学的特征。

Subacut myeloid leukemia can be a defined type of leukemia. The common characteristics of subacute myeloid leukemia are as follows: the onset is insidious, and anemia and hemorrhage of skin and mucosa are the main clinical manifestations. Hepatosplenomegaly is rare. There are multilineage abnormalities in blood cell counts and increased blasts in the bone marrow with cytogenetical abnormal clone in most cases. The disease course is subacute and progressive.

1、亚急性髓性白血病是一个可以确定的白血病类型，其特征为：起病隐袭，以贫血或皮肤粘膜出血为主要症状，肝脾肿大的特征较少，血象为一系、二系或三系的异常，骨髓细胞形态学检查原早幼粒细胞异常增高，细胞遗传学检查多数有克隆性异常核型，病程中可有克隆演进，呈现亚急性而进行性的临床经过。

Objective To investigate the cytologic characters of low dose iron supplementation in children with iron deficiency anemia of children.

目的：探讨小剂量间断补铁治疗小儿轻度缺铁性贫血的临床效果及其细胞学分析。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。