家族性低钾性周期性麻痹1例报告

Gokmen Ozceylan, D. Toprak
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引用次数: 0

摘要

低钾性周期性麻痹是一种先天性疾病,其特点是间歇性发作的肌肉无力或麻痹。发作可以每天发生,也可以一年发生一次,可能持续几个小时,也可能持续几天。发作时血清钾水平很低。但两次发作之间的血钾水平是正常的。全身不缺钾。本文报告了一名16岁男孩,其祖父、父亲和叔叔均有相同的症状,并根据临床和实验室特征,在一次大运动后首次发作家族性低钾性周期性麻痹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Familial Hypokalemic Periodic Paralysis: Case Report
Hypokalemic periodic paralysis is a congenital disorder which is characterized by intermittent episodes of muscle weakness or paralysis. The attacks can occur everyday or once a year, may last for a few hours or for several days. Serum potassium level is low during the attack. But serum potassium levels are normal between two attacks. There is no potassium deficiency in the whole body. In this report, a 16 years old boy, whose grandfather, father and uncle had the same semptoms, and had his first attack of familial hypokalemic periodic paralysis following a grand exercise were presented according to the clinical and laboratory features.
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