نتایج جستجو برای: hypokalemic periodic paralysis

تعداد نتایج: 101793  

2014
June-Bum Kim

Channelopathies are a heterogeneous group of disorders resulting from the dysfunction of ion channels located in the membranes of all cells and many cellular organelles. These include diseases of the nervous system (e.g., generalized epilepsy with febrile seizures plus, familial hemiplegic migraine, episodic ataxia, and hyperkalemic and hypokalemic periodic paralysis), the cardiovascular system...

Journal: :Thyroid : official journal of the American Thyroid Association 2011
Takao Ando Tomoko Henmi Daisuke Haruta Ai Haraguchi Ikuko Ueki Ichiro Horie Misa Imaizumi Toshiro Usa Kouji Maemura Atsushi Kawakami

BACKGROUND Thyrotoxicosis is known to be associated with sinus tachycardia and supraventricular tachyarrhythmias, but rarely with ventricular fibrillation (Vf), which has only occurred in some patients with hypokalemic periodic paralysis or ischemic heart disease. PATIENT FINDINGS We present three men who were transferred to our hospital with Graves' disease who developed idiopathic Vf. None ...

2012
Yi-Chu Lin Che-Wei Wu Hui-Chun Chen Hsiu-Ya Chen I-Cheng Lu Cheng-Jing Tsai Wen-Rei Kuo Feng-Yu Chiang

Thyrotoxic hypokalemic periodic paralysis (THPP) is a rare, potentially life-threatening endocrine emergency. It is characterized by recurrent muscle weakness and hypokalemia. Because many THPP patients do not have obvious symptoms and signs of hyperthyroidism, misdiagnosis may occur. The published studies revealed that definitive therapy for THPP is control of hyperthyroidism by medical therap...

Journal: :Anesthesia and analgesia 1994
K Jurkat-Rott F Lehmann-Horn A Elbaz R Heine R G Gregg K Hogan P A Powers P Lapie J E Vale-Santos J Weissenbach

The only calcium channel mutation reported to date is a deletion in the gene for the DHP-receptor alpha 1-subunit resulting in neonatal death in muscular dysgenesis mice (1). In humans, this gene maps to chromosome 1q31-32. An autosomal dominant muscle disease, hypokalemic periodic paralysis (HypoPP), has been mapped to the same region (2). Sequencing of cDNA of two patients revealed a G-to-A b...

Journal: :Canadian Journal of Anesthesia/Journal canadien d'anesthésie 2000

Journal: :Current neurology and neuroscience reports 2012
James A Burge Michael G Hanna

The nondystrophic myotonias and primary periodic paralyses are an important group of genetic muscle diseases characterized by dysfunction of ion channels that regulate membrane excitability. Clinical manifestations vary and include myotonia, hyperkalemic and hypokalemic periodic paralysis, progressive myopathy, and cardiac arrhythmias. The severity of myotonia ranges from severe neonatal presen...

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