Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Napoli, Italy.
CEINGE Biotecnologie Avanzate, Napoli, Italy.
Am J Hematol. 2018 Jan;93(1):107-121. doi: 10.1002/ajh.24929. Epub 2017 Oct 23.
Hereditary stomatocytoses are a wide class of hemolytic anemias characterized by alterations of ionic flux with increased cation permeability that results in inappropriate shrinkage or swelling of the erythrocytes, and water lost or gained osmotically. The last few years have been crucial for new acquisitions in this field in terms of identifying new causative genes and of studying their pathogenetic mechanisms. This review summarizes the main features of erythrocyte membrane transport diseases, dividing them into forms with either isolated erythroid phenotype (nonsyndromic) or extra-hematological manifestations (syndromic), and focusing particularly on the most recent advances regarding dehydrated forms of hereditary stomatocytosis and familial pseudohyperkalemia.
遗传性口形红细胞增多症是一类广泛的溶血性贫血,其特征为离子流改变,阳离子通透性增加,导致红细胞的不适当收缩或肿胀,以及渗透性地失去或获得水分。在过去的几年中,在确定新的致病基因和研究其发病机制方面,该领域取得了新的突破。本综述总结了红细胞膜转运疾病的主要特征,将其分为单纯红系表型(非综合征性)或非血液学表现(综合征性),并特别关注遗传性口形红细胞增多症和家族性假性高钾血症的脱水形式的最新进展。