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Acanthocytosis--biochemical and physiological considerations.

作者信息

Biemer J J

出版信息

Ann Clin Lab Sci. 1980 May-Jun;10(3):238-49.

PMID:6994580
Abstract

Acanthocytosis represents an unusually pathological variant of red cell morphology which is encountered in a diverse group of inherited and acquired disease states. While the morphological features are similar in all instances, the biochemical lesions frequently differ. Most demonstrable abnormalities involve lipids although those acanthocytes associated with the McLeod phenotype are probably due to an alteration in a membrane protein. Acanthocytes, regardless of their etiology, usually have a decreased survival in the circulation owing to splenic sequestration and destruction.

摘要

相似文献

1
Acanthocytosis--biochemical and physiological considerations.
Ann Clin Lab Sci. 1980 May-Jun;10(3):238-49.
2
Acanthocytosis and neurological impairment--a review.棘红细胞增多症与神经功能障碍——综述
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A basis of the acanthocytosis in inherited and acquired disorders.遗传性和获得性疾病中棘红细胞增多症的一个基础。
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Decreased fluidity of red cell membrane lipids in abetalipoproteinemia.无β脂蛋白血症时红细胞膜脂质流动性降低。
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[Abetalipoproteinemia and acanthocytosis in a 3-month-old infant].[一名3个月大婴儿的无β脂蛋白血症和棘红细胞增多症]
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[Reversible acquired acanthocytosis and hemolytic anemia associated with hypobetalipoproteinemia in a chronic alcoholic].
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Acanthocytosis and neurological disorders.棘红细胞增多症与神经系统疾病。
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Clinical features and molecular bases of neuroacanthocytosis.神经棘红细胞增多症的临床特征及分子基础
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Hereditary acanthocytosis associated with the McLeod phenotype of the Kell blood group system.
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引用本文的文献

1
Impaired Cytoskeletal and Membrane Biophysical Properties of Acanthocytes in Hypobetalipoproteinemia - A Case Study.低β脂蛋白血症棘形红细胞的细胞骨架和膜生物物理特性受损——病例研究
Front Physiol. 2021 Feb 23;12:638027. doi: 10.3389/fphys.2021.638027. eCollection 2021.
2
Single red blood cell analysis reveals elevated hemoglobin in poikilocytes.单个红细胞分析显示异形红细胞中血红蛋白升高。
J Biomed Opt. 2020 Jan;25(1):1-13. doi: 10.1117/1.JBO.25.1.015004.
3
Mechanism of red blood cell acanthocytosis and echinocytosis in vivo.体内红细胞棘形红细胞增多症和棘状红细胞增多症的机制。
J Membr Biol. 1984;77(2):153-9. doi: 10.1007/BF01925863.
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Clinicopathologic correlation and pathogenesis of ocular and central nervous system manifestations in Hallervorden-Spatz syndrome.
Acta Neuropathol. 1992;83(2):113-9. doi: 10.1007/BF00308470.