Department of Biomedical and NeuroMotor Sciences, Alma Mater Studiorum-University of Bologna, Bologna, Italy.
IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Epileptic Disord. 2023 Jun;25(3):410-415. doi: 10.1002/epd2.20039. Epub 2023 Apr 27.
Cryohydrocytosis is a form of stomatocytosis characterized by the leakage of sodium and potassium from red blood cells at low temperatures, characterized by pseudohyperkalemia. Stomatin-deficient cryohydrocytosis is an extremely rare variant that only recently has been related to pathogenic variants in the SLC2A1 gene, encoding the main glucose transporter of the blood-brain barrier and red blood cells, GLUT1. It follows that GLUT1 deficiency syndrome, a rare but significant cause of metabolic epilepsy, may present with stomatin-deficient cryohydrocytosis, although this correlation has only been reported in a few instances. We present the case of a patient carrying a novel de novo SLC2A1 pathogenic variant presenting with GLUT1 deficiency syndrome, pseudohyperkalemia, and splenomegaly consistent with cryohydrocytosis. We also review the previously reported cases of stomatin-deficient cryohydrocytosis in the literature. As highlighted by our case, elevated potassium levels are a cause of concern, and GLUT1 deficiency syndrome patients are thus at risk of being subjected to unnecessary examinations; pseudohyperkalemia may be underrecognized in clinical practice.
Cryohydrocytosis 是一种以红细胞在低温下渗漏钠和钾为特征的口形红细胞增多症,其特征为假性高钾血症。缺乏 stomatin 的 cryohydrocytosis 是一种极其罕见的变体,最近才与编码血脑屏障和红细胞主要葡萄糖转运体 GLUT1 的 SLC2A1 基因的致病性变异相关。因此,GLUT1 缺乏综合征是一种罕见但重要的代谢性癫痫病因,可能表现为缺乏 stomatin 的 cryohydrocytosis,尽管这种相关性仅在少数情况下有报道。我们报告了一例携带新的从头 SLC2A1 致病性变异的患者,该患者表现为 GLUT1 缺乏综合征、假性高钾血症和脾肿大,符合 cryohydrocytosis。我们还回顾了文献中以前报道的缺乏 stomatin 的 cryohydrocytosis 病例。正如我们的病例所强调的,高钾血症是一个值得关注的原因,因此 GLUT1 缺乏综合征患者有接受不必要检查的风险;假性高钾血症在临床实践中可能未被充分认识。