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Updated: Jul 21, 2026

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Measuring Glucose Uptake in Drosophila Models of TDP-43 Proteinopathy
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通过全基因组测序揭开葡萄糖酸盐异构酶缺乏症:一个案例报告
Sissel Holme1, Richard van Wijk2, Andreas Ørslev Rasmussen3
1Danish Red Blood Cell Center, Department of Hematology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Journal of medical case reports
|March 28, 2024
概括
葡萄糖-6-酸盐异构酶缺乏导致遗传性贫血. 全基因组测序发现了新的变异,有助于诊断和管理这种罕见的糖质酶酶病变.
科学领域:
- 遗传学 遗传学 是一个
- 生物化学 生物化学
背景情况:
- 葡萄糖-6-酸盐异构酶 (GPI) 缺乏症是一种罕见的遗传疾病.
- 它会导致遗传性非球球性溶血性贫血,第二个最常见的红细胞甘油性酵素病变.
- 全球报告的病例约为90例,症状从贫血到严重的神经障碍等各异.
相关概念视频
Glucose Transporters
Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Inborn Errors of Metabolism
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...

