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[遗传性球形红细胞增多症:红细胞膜蛋白的一年研究]

[Hereditary spherocytosis: one year study of erythrocyte membrane proteins].

作者信息

Tshilolo L, Kagambega F, Sztern B, Vertongen F, Gulbis B

机构信息

Laboratoire de Chimie Clinique, Hôpital Erasme.

出版信息

Rev Med Brux. 1998 Oct;19(5 Pt 1):417-23.

PMID:9844481
Abstract

Hereditary spherocytosis (HS) is a congenital hemolytic anemia which affects one person out of 5000 in Northern Europe. HS is caused by defects of the red cell membrane proteins involving mainly ankyrin or band 3, and less frequently, protein 4.2 or spectrin. The reduction of red cell osmotic resistance and the recognition of spherocytes on the peripheral blood smear are the primary laboratory tests necessary to evocate a diagnosis of hereditary spherocytosis. Analysis of the red cell membrane proteins using polyacrylamide gel electrophoresis is used to quantify individual proteins and to identify the protein defect related to a diagnosis of HS. Samples from 47 patients and 25 controls were studied by electrophoresis of the red cell membrane proteins. Protein deficiencies related to HS were demonstrated for 21 patients. In 4 other cases, abnormalities of membrane proteins unrelated to HS were also demonstrated. Electrophoresis of the red cell membrane proteins allows the identification of the protein deficiency related to HS and thus confirms the diagnosis of HS, but also points to the underlying molecular defect, the inheritance pattern and the clinical aspects of the disease.

摘要

遗传性球形红细胞增多症(HS)是一种先天性溶血性贫血,在北欧每5000人中就有1人受其影响。HS是由红细胞膜蛋白缺陷引起的,主要涉及锚蛋白或带3蛋白,较少见的是蛋白4.2或血影蛋白。红细胞渗透抵抗力降低以及在外周血涂片上识别球形红细胞是做出遗传性球形红细胞增多症诊断所需的主要实验室检查。使用聚丙烯酰胺凝胶电泳分析红细胞膜蛋白可对单个蛋白进行定量,并识别与HS诊断相关的蛋白缺陷。通过红细胞膜蛋白电泳对47例患者和25例对照的样本进行了研究。21例患者显示出与HS相关的蛋白缺乏。在另外4例病例中,还显示出与HS无关的膜蛋白异常。红细胞膜蛋白电泳不仅可以识别与HS相关的蛋白缺乏从而确诊HS,还能指出潜在的分子缺陷、遗传模式以及该疾病的临床特征。

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