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非典型遗传性血影细胞球形红细胞增多症表型伴假性低血钾和 3 带蛋白的一种新变异。

Atypical hereditary spherocytosis phenotype associated with pseudohypokalaemia and a new variant in the band 3 protein.

机构信息

Biochemistry, Worcestershire Acute Hospitals NHS Trust, Worcester, UK

出版信息

BMJ Case Rep. 2020 Dec 9;13(12):e238428. doi: 10.1136/bcr-2020-238428.

Abstract

Red blood cell (RBC) membrane disorders are predominantly caused by mutations resulting in decreased RBC deformability and permeability. We present a family in which, the proband and his daughter presented with pseudohypokalaemia. Studies on the temperature dependence of pseudohypokalaemia suggested a maximum decrease in serum potassium when whole blood is stored at 37°C. Routine haematology suggested mild haemolysis with a hereditary spherocytosis phenotype. These two cases present a novel variant in temperature-dependent changes in potassium transport. A new variant was identified in the SLC4A1 gene which codes for band 3 protein (anion exchanger 1) in RBC membrane which may contribute to the phenotype. This is the first report of familial pseudohypokalaemia associated with changes in RBC membrane morphology. The clinical implications of pseudohypokalaemia are that it can lead to inappropriate investigation or treatment. However, many questions remain to be solved and other RBC membrane protein genes should be studied.

摘要

红细胞(RBC)膜疾病主要由导致 RBC 变形能力和通透性降低的突变引起。我们介绍了一个家系,该家系中的先证者和他的女儿表现为假性低血钾症。对假性低血钾症温度依赖性的研究表明,当全血在 37°C 下储存时,血清钾的下降幅度最大。常规血液学检查提示存在轻微的溶血性贫血,表现为遗传性球形红细胞增多症。这两个病例表现出钾转运温度依赖性变化的新型变异。在 SLC4A1 基因中发现了一个新的变异,该基因编码 RBC 膜上的带 3 蛋白(阴离子交换蛋白 1),这可能导致了该表型。这是首例与 RBC 膜形态变化相关的家族性假性低血钾症的报道。假性低血钾症的临床意义在于它可能导致不适当的检查或治疗。然而,仍有许多问题需要解决,应该研究其他 RBC 膜蛋白基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f57/7733106/c3d5b1c9ab24/bcr-2020-238428f01.jpg

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