丙酮酸激酶缺乏:差一点

M. Tullu, Ankita A. Kulkarni, Mukesh Agrawal
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引用次数: 4

摘要

丙酮酸激酶缺乏症是一种遗传性疾病,会影响将氧气输送到身体组织的红细胞。患有这种疾病的人患有一种被称为慢性溶血性贫血的疾病,在这种疾病中,红细胞过早被分解(发生溶血),导致红细胞短缺(贫血)。具体来说,丙酮酸激酶缺乏是一种称为遗传性非球型溶血性贫血的遗传性溶血性贫血的常见原因。在遗传性非球形溶血性贫血中,红细胞不像其他形式的溶血性贫血那样呈球形。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyruvate Kinase Deficiency: A Near Miss
Pyruvate kinase deficiency is an inherited disorder that affects red blood cells, which carry oxygen to the body's tissues. People with this disorder have a condition known as chronic hemolytic anemia, in which red blood cells are broken down (undergo hemolysis) prematurely, resulting in a shortage of red blood cells (anemia). Specifically, pyruvate kinase deficiency is a common cause of a type of inherited hemolytic anemia called hereditary nonspherocytic hemolytic anemia. In hereditary nonspherocytic hemolytic anemia, the red blood cells do not assume a spherical shape as they do in some other forms of hemolytic anemia.
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