1) Hypokalemic periodic paralysis
低钾型周期性麻痹
1.
Objective To find if the mutations that had been reported abroad exist in a patient with hypokalemic periodic paralysis.
目的探讨低钾型周期性麻痹患者是否存在相关基因的突变。
2.
Object: Hypokalemic periodic paralysis has gene disorders in chromosomes.
目的:低钾型周期性麻痹为一种常染色体发生基因突变的疾病,可以是由遗传获得性的突变基因,少数病例也可以是因受孕时生殖细胞发生基因突变而产生。
2) hypokalemic periodic paralysis
低血钾型周期性麻痹
1.
Results Six cases of FPP were diagnosed as hypokalemic periodic paralysis,and all occured as an autosomal do.
结果6例为家族性低血钾型周期性麻痹,具有常染色体显性遗传的特征;发作时血清钾1。
3) Hypokalemic periodic paralysis
低钾性周期性麻痹
1.
Hypokalemic periodic paralysis: report of a Chinese pedigree with a novel mutation site in SCN4A gene;
目的 通过检测相关基因的突变位点来研究低钾性周期性麻痹 (HOKPP)这一常染色体显性遗传疾病的遗传学病因。
4) low-potassium periodic paralysis of human
人低钾周期性麻痹
1.
CACNA1S gene was the coding gene of α1 subunit of L-type calcium channel,its mutation would induce low-potassium periodic paralysis of human and high-temperature syndrom of pig.
CACNA1S基因是L-型钙离子通道α1亚单位的编码基因,CACNA1S的基因突变会引起人低钾周期性麻痹及猪高温综合症,有关研究推测该基因是影响猪肉质性状的候选基因。
6) normokalemic periodic paralysis
正常血钾型周期性麻痹
1.
The mutation V781I in SCN4A gene exists in Chinese patients with normokalemic periodic paralysis;
正常血钾型周期性麻痹存在SCN4A基因V781I突变
补充资料：周期性麻痹
周期性麻痹
periodic paralysis
一种周期性发作的肌弛缓性瘫痪病。每次发作迅速，于短期内缓解，或痊愈以及发作时血清钾降低是本病的特点。瘫痪常以肢体近端为重，左右对称，偶有单侧肢体瘫痪者。其症状常在1～2小时内达到高峰。瘫痪持续数小时或数日后可自行缓解。无感觉障碍。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条