نتایج جستجو برای: myotonia

تعداد نتایج: 1446  

Journal: :Genetics Selection Evolution 1997

Journal: :Journal of Veterinary Internal Medicine 1998

Journal: :Acta anaesthesiologica Scandinavica 2003
E Farbu E Søfteland L A Bindoff

Myotonia congenita (MC) is caused by a defect in the skeletal muscle chloride channel function, which may cause sustained membrane depolarisation. We describe a previously healthy 32-year-old woman who developed a life-threatening muscle spasm and secondary ventilation difficulties following a preoperative injection of suxamethonium. The muscle spasms disappeared spontaneously and the surgery p...

2013
Michinori Koebis Tamami Kiyatake Hiroshi Yamaura Kanako Nagano Mana Higashihara Masahiro Sonoo Yukiko Hayashi Yoichi Negishi Yoko Endo-Takahashi Dai Yanagihara Ryoichi Matsuda Masanori P. Takahashi Ichizo Nishino Shoichi Ishiura

Phosphorodiamidate morpholino oligonucleotide (PMO)-mediated control of the alternative splicing of the chloride channel 1 (CLCN1) gene is a promising treatment for myotonic dystrophy type 1 (DM1) because the abnormal splicing of this gene causes myotonia in patients with DM1. In this study, we optimised a PMO sequence to correct Clcn1 alternative splicing and successfully remedied the myotonic...

Journal: :BMC Neurology 2003
Nicola C Ho Stacey Sandusky Victor Madike Clair A Francomano Marinos C Dalakas

BACKGROUND Chondrodystrophic myotonia or Schwartz-Jampel syndrome is a rare genetic disorder characterized by myotonia and skeletal dysplasia. It may be progressive in nature. Recently, the gene responsible for Schwartz-Jampel syndrome has been found and the defective protein it encodes leads to abnormal cartilage development and anomalous neuromuscular activity. CASE PRESENTATION We report t...

Journal: :Neuroscience letters 2011
Akira Tsujino Muneshige Kaibara Hideki Hayashi Hiroto Eguchi Susumu Nakayama Katsuya Sato Taku Fukuda Yohei Tateishi Susumu Shirabe Kohtaro Taniyama Atsushi Kawakami

Myotonia congenita is caused by mutation of the CLCN1 gene, which encodes the human skeletal muscle chloride channel (ClC-1). The ClC-1 protein is a dimer comprised of two identical subunits each incorporating its own separate pore. However, the precise pathophysiological mechanism underlying the abnormal ClC-1 channel gating in some mutants is not fully understood. We characterized a ClC-1 mut...

Journal: :Clinical genetics 2011
C Sun M Van Ghelue L Tranebjærg F Thyssen Ø Nilssen T Torbergsen

Myotonia is characterized by hyperexcitability of the muscle cell membrane. Myotonic disorders are divided into two main categories: non-dystrophic and dystrophic myotonias. The non-dystrophic myotonias involve solely the muscle system, whereas the dystrophic myotonias are characterized by multisystem involvement and additional muscle weakness. Each category is further subdivided into different...

Journal: :Human molecular genetics 1998
C Kubisch T Schmidt-Rose B Fontaine A H Bretag T J Jentsch

Mutations in the ClC-1 muscle chloride channel cause either recessive or dominant myotonia congenita. Using a systematic screening procedure, we have now identified four novel missense mutations in dominant (V286A, F307S) and recessive myotonia (V236L, G285E), and have analysed the effect of these and other recently described mutations (A313T, I556N) on channel properties in the Xenopus oocyte ...

Journal: :Proceedings of the Royal Society of Medicine 1935

Journal: :The Journal of clinical investigation 2008
Lawrence J Hayward Joanna S Kim Ming-Yang Lee Hongru Zhou Ji W Kim Kumudini Misra Mohammad Salajegheh Fen-fen Wu Chie Matsuda Valerie Reid Didier Cros Eric P Hoffman Jean-Marc Renaud Stephen C Cannon Robert H Brown

Hyperkalemic periodic paralysis (HyperKPP) produces myotonia and attacks of muscle weakness triggered by rest after exercise or by K+ ingestion. We introduced a missense substitution corresponding to a human familial HyperKPP mutation (Met1592Val) into the mouse gene encoding the skeletal muscle voltage-gated Na+ channel NaV1.4. Mice heterozygous for this mutation exhibited prominent myotonia a...

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