hereditary spherocytosis
释义
遗传性球形红细胞性贫血；
权威例句
Hereditary SpherocytosisHereditary Spherocytosis
Hereditary spherocytosis.
HEREDITARY SPHEROCYTOSIS; CLINICAL FAMILY STUDIES.
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer
Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: a case report and review of the literature.
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
Guidelines for the diagnosis and management of hereditary spherocytosis.
Fine structure of the red pulp of the spleen in hereditary spherocytosis
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
PARENTAL MOSAICISM FOR ANKYRIN-1 MUTATIONS IN TWO FAMILIES WITH HEREDITARY SPHEROCYTOSIS (HS)
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.
1. The sinusoids are packed with RBC's in this case of hereditary spherocytosis. The osmotic fragility of spherocytes is increased, because the RBC's have decreased surface area per unit volume.
遗传性球形红细胞增多症中，窦状隙被RBC塞满，球形红细胞的渗透性脆性增加，因为RBC每单位体积的表面积减少。
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2. Objective to analyze the causes of misdiagnosis and missed diagnosis in hereditary spherocytosis (HS) and improve the diagnosis rate.
目的分析遗传性球形红细胞增多症(HS)误诊、漏诊原因，以提高其诊断率。
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3. Objective to explore the feasibility and the efficacy of laparoscopic splenectomy of massive splenomegaly in the treatment of hereditary spherocytosis in children.
目的探讨腹腔镜巨脾切除术在小儿遗传性球形红细胞增多症治疗中的可行性及效果评价。
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4. There is a rare condition known as hereditary spherocytosis.
这是极少见的遗传性球形红细胞增多症。
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5. Objective to analyze the clinical feature of children hereditary spherocytosis (HS).
目的分析儿童遗传性球形红细胞增多症的临床特点。
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6. Objective to analyze the clinical feature of children hereditary spherocytosis (HS).
目的分析儿童遗传性球形红细胞增多症的临床特点。
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hereditary spherocytosis
