1) congenital dyserythropoietic anemia-type Ⅰ
先天性红细胞生成障碍性贫血Ⅰ型
3) Pure red cell aplasia
纯红细胞再生障碍性贫血
1.
Thymoma associated with pure red cell aplasia: a cases report and review of Chinese literatures;
胸腺瘤合并单纯红细胞再生障碍性贫血1例及文献复习
2.
Clinic analysis of 24 cases with pure red cell aplasia;
24例纯红细胞再生障碍性贫血临床分析
3.
Objective:To investigate the diagnosis, etiology, pathogenesis and therapy of pure red cell aplasia (PRCA).
目的 :探讨纯红细胞再生障碍性贫血的病因、发病机制、诊断和治疗。
4) pure red cell aplasia (PRCA)
单纯红细胞再生障碍性贫血
1.
Objective: to understand the pathogenesis , clinical features, methodes of diagnosis of thymoma associated with pure red cell aplasia (PRCA) and to evaluate the outcome of the therapy.
目的 探讨胸腺瘤合并单纯红细胞再生障碍性贫血的发病机理、临床表现、诊断方法和有效的治疗方法。
5) thalassemia
[英][,θælə'si:miə] [美][,θælə'simɪə]
珠蛋白生成障碍性贫血
1.
Application Values of Red Blood Cell MCV and RDW in Preliminary Screening Diagnosis of Thalassemia;
红细胞MCV与RDW在初筛诊断珠蛋白生成障碍性贫血的应用价值
2.
Quantitative analysis of HbA_2 with high-performance liquid chromatography in thalassemia screening;
高效液相色谱法定量分析HbA_2在珠蛋白生成障碍性贫血筛查中的应用
3.
Objective To study the clinical significance of decreasing febrile non hemolytic transfusion reaction(FNHTR) by infusion erythrocyte after filtering leukocyte in children with β thalassemia major.
目的了解滤白细胞红细胞(滤白)输注对降低重型β珠蛋白生成障碍性贫血(重型β地贫)患儿非溶血性发热性输血反应(FNHTR)的意义。
6) Severe aplastic anemia
重型再生障碍性贫血
1.
Allogeneic hematopoietic stem cell transplantation with HLA-matched sibling and haploidentical donor for multitransfused severe aplastic anemia;
HLA匹配同胞供者和半倍体供者异基因造血干细胞移植治疗多次输血的重型再生障碍性贫血
2.
Objective To observe the curative effect of the therapy of replenishing qi and blood combined with stanozolol on severe aplastic anemia.
目的观察益气养血补肾法治疗重型再生障碍性贫血的临床疗效。
3.
Objective To evaluate the safety measures for children with severe aplastic anemia, treated by the combination of human immunoglobulin and cyclosporin A.
目的探讨采用抗人胸腺免疫球蛋白联合环孢素A治疗重型再生障碍性贫血患儿副反应的安全防护措施。
补充资料：先天性唇裂
先天性唇裂
congenital cleft lip
俗称“兔唇”。在面裂中最为常见。发病率约为0.1%，绝大多数发生在上唇的一侧或两侧，以单侧多见，左侧多于右侧。发生在上、下唇的正中裂极为罕见。根据裂隙的部位可分为部分裂及完全裂两种。仅有口轮匝肌发育不全，皮肤和黏膜完整且呈线状凹陷时称为皮下裂或隐裂。唇裂与腭裂可同时存在，少数可伴有身体其他部位的畸形。唇裂发生的原因与遗传、环境等多因素有关。在胚胎发育过程中，上颌突在第7周时未能与球状突融合时可发生本病。两个球状突未能融合则发生上唇正中裂，两个下颌突未融合则发生下唇正中裂。发生唇裂时不仅损害面部容貌的完整，且影响吮吸、妨碍发音和牙槽弓的发育。因此应在出生后3个月左右进行手术修复。唇裂手术基本原则相同，但手术方法很多，各有优、缺点。应根据具体情况选用适合的方法，以尽量达到恢复上唇的形态、吮吸、发音等正常功能的目的。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条