نتایج جستجو برای: myotonia

تعداد نتایج: 1446  

Journal: :Anaesthesia and Intensive Care 2001

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1988

Journal: :The Boston Medical and Surgical Journal 1908

Journal: :The Journal of clinical investigation 2007
Thurman M Wheeler John D Lueck Maurice S Swanson Robert T Dirksen Charles A Thornton

In myotonic dystrophy (dystrophia myotonica [DM]), an increase in the excitability of skeletal muscle leads to repetitive action potentials, stiffness, and delayed relaxation. This constellation of features, collectively known as myotonia, is associated with abnormal alternative splicing of the muscle-specific chloride channel (ClC-1) and reduced conductance of chloride ions in the sarcolemma. ...

Journal: :The Biochemical journal 2007
María J Macías Oscar Teijido Giovanni Zifarelli Pau Martin Ximena Ramirez-Espain Antonio Zorzano Manuel Palacín Michael Pusch Raúl Estévez

Myotonia is a state of hyperexcitability of skeletal-muscle fibres. Mutations in the ClC-1 Cl- channel cause recessive and dominant forms of this disease. Mutations have been described throughout the protein-coding region, including three sequence variations (A885P, R894X and P932L) in a distal C-terminal stretch of residues [CTD (C-terminal domain) region] that are not conserved between CLC pr...

Journal: :Pediatrics 2013
Emilie Caietta Mathieu Milh Damien Sternberg Anne Lépine Christophe Boulay Aileen McGonigal Brigitte Chabrol

Mutations of SCN4A encoding the skeletal muscle sodium channel Nav 1.4 cause several types of disease, including sodium channel myotonias. The latter may be responsible for neonatal symptoms, including severe neonatal episodic laryngospasm (SNEL). Establishing the diagnosis of SCN4A-related SNEL early in the neonatal period is crucial because treatment is available that can reduce laryngospasm ...

Journal: :JAMA 2012
Jeffrey M Statland Brian N Bundy Yunxia Wang Dipa Raja Rayan Jaya R Trivedi Valeria A Sansone Mohammad K Salajegheh Shannon L Venance Emma Ciafaloni Emma Matthews Giovanni Meola Laura Herbelin Robert C Griggs Richard J Barohn Michael G Hanna

CONTEXT Nondystrophic myotonias (NDMs) are rare diseases caused by mutations in skeletal muscle ion channels. Patients experience delayed muscle relaxation causing functionally limiting stiffness and pain. Mexiletine-induced sodium channel blockade reduced myotonia in small studies; however, as is common in rare diseases, larger studies of safety and efficacy have not previously been considered...

Journal: :British journal of anaesthesia 1995
E Abouleish

Sir,—We read with interest the review article on anaesthesia and myotonia [1]. Myotonia dystrophica is an uncommon disorder with as yet no consensus of opinion regarding the ideal anaesthetic for these patients. Propofol has been used in this disorder with variable responses, including prolonged recovery, altered dose–response curves and precipitation of the myotonia. We report three additional...

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