Methods: The clinical manifestation, accessory examination, and therapeutic methods of30 cases with hypokalemic periodic paralysis were analyzed. 方法:分析30例低血钾麻痹病人的临床表现、辅助检查及治疗方法。
Effect of ion channels on attack of hypokalemic periodic paralysis 离子通道对低钾性周期性麻痹发病的影响
Clinical and pathological study on hypokalemic periodic paralysis 低钾型周期性麻痹的临床及病理研究
Health Education to Patients with Hypokalemic Periodic Paralysis 低钾型周期性麻痹病人的健康教育
The Clinical Experience of Diagnosis and Treatment about Hypokalemic Periodic Paralysis ( 96 cases) 低钾型周期性麻痹急诊处理体会(附96例报道)
Objective To investigate the clinical significance of individual nursing care in treating hypokalemic periodic paralysis. 目的探讨个体化护理对治疗低血钾型周期性麻痹的意义。
Methods Blood potassium, NO and NOS were measured in patients with hypokalemic periodic paralysis during paralysis stroke and after muscle power recovered. 方法低钾型周期性麻痹患者,在弛缓性瘫痪发作期及肌力恢复后,同时检测血钾、NO、一氧化氮合酶(NOS)。
Conclusion GS may be present with severe hypocalcaemia and hypokalemic periodic paralysis; the renal clearance studies by diuretic administration may be of help in diagnosing Gitelman's syndrome, and the combined use of indomethacin with triamterene has good therapeutic effect. GS可伴有严重低钙血症、周期性麻痹,肾脏清除率试验在临床上可帮助诊断,消炎痛及氨苯蝶啶联合应用治疗有效。
A Clinical Analysis of 40 Cases with Hypokalemic Paralysis 低钾性瘫痪40例临床分析
Gene Analysis on Hypokalemic Periodic Paralysis 低钾型周期性麻痹症的基因分析
Objective To explore the genetic pathogenesis of hypokalemic periodic paralysis ( HOKPP), an autosomal dominant disease by detecting gene mutation at related loci. 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。
Genetic Research of Ion Channel Gene Mutations and Clinical Study on Primary Hypokalemic Periodic Paralysis 原发性低钾型周期性麻痹的离子通道基因突变及临床研究
Bartter syndrome is a group of inherited renal tubular disorders characterized by hypokalemic metabolic alkalosis. Bartter综合征是一组以低钾性代谢性碱中毒为主要特征的遗传性肾小管疾病。
Conclusions The study indicates that individual nursing care has a high clinical value of diagnosis and treatment in hypokalemic periodic paralysis. 结论个体化护理对低血钾型周期性麻痹的诊断及治疗有着极其重要的作用。
Conclusion The heredity in hypokalemic periodic paralysis is of genetic heterogeneity. 结论低钾性周期性麻痹的遗传存在异质性。
Hypokalemic periodic paralysis was present in 6 cases. 6例并发低钾性周期性麻痹。
Objective: The diagnosis and treatment of hypokalemic paralysis were discussed. 目的:探讨低钾性瘫痪的诊断及治疗。
Results There were only 4 cases of primary hypokalemic periodic paralysis, while 86.7% ( 26/ 30) were secondary hypokalemia caused by various other diseases. 结果原发于低钾周期性麻痹仅4例,86.7%(26/30)的低钾血症为多种病因继发的结果。
Objective To investigate the association between serum potassium ion concentration and the degree of paralysis, and the effect of sylvite supplementary treatment in patients who suffered from hypokalemic periodic paralysis ( HoPP). 目的研究低钾型周期性瘫痪(HoPP)患者血清钾离子浓度与肢体瘫痪程度的关系及对补钾治疗的影响。
Objective To discuss the changes of ECG and cardiac enzyme spectrum during hypokalemic periodicit paralysis. 目的探讨低钾型周期性麻痹的心电图(ECG)改变与心肌酶谱变化。
Nursing care of one patient with familial hypokalemic periodic paralysis 1例家族性低钾型周期性麻痹患者的护理指导
The Diagnosis and Emergency treatment of Paralysis of the Respiratory Muscles due to Hypokalemic Periodic Paralysis 低钾性周期性麻痹所致呼吸肌麻痹的及时诊断与抢救
After the operation, the hypokalemic myopathy oc curred in 1 case, urinary tract infection in 2 cases, adhesive intestinal obstruction in 1 case, urinary bladder stone in 2 cases, and stenosis of anastomosis between the kidney and intestine in 1 case. 结果术后并发低血钾性肌病1例,尿路感染2例,经药物治愈;并发粘连性肠梗阻1例,膀胱结石2例,肾肠吻合口狭窄1例,均再手术治愈。
Hypokalemic periodic paralysis and channelopathy 低钾性周期性麻痹与离子通道病
Studies on Hypokalemic Flabbiness Disease 低血钾软病的研究
It was found that many patients were relatives in a family. So it was also called Familial hypokalemic periodic paralysis. 由于大多数低钾型周期性麻痹患者发现具有家族史,故又称为家族性低钾型周期性麻痹,遗传方式为常染色体显性遗传。
Conclusion: The mutations have been studied were not found in the Hypokalemic periodic paralysis patient. 结论:本实验中低钾型周期性麻痹患者未发现预期研究的相关突变基因。