Guidelines on clinical presentation and management of nondystrophic myotonias

被引:49
|
作者
Stunnenberg, Bas C. [1 ]
LoRusso, Samantha [2 ]
Arnold, W. David [2 ]
Barohn, Richard J. [3 ]
Cannon, Stephen C. [4 ]
Fontaine, Bertrand [5 ,6 ]
Griggs, Robert C. [7 ]
Hanna, Michael G. [8 ]
Matthews, Emma [8 ]
Meola, Giovanni [9 ,10 ]
Sansone, Valeria A. [10 ,11 ]
Trivedi, Jaya R. [12 ]
van Engelen, Baziel G. M. [1 ]
Vicart, Savine [5 ]
Statland, Jeffrey M. [3 ]
机构
[1] Radboud Univ Nijmegen, Dept Neurol, Med Ctr, Nijmegen, Netherlands
[2] Ohio State Univ, Dept Neurol, Wexner Med Ctr, Columbus, OH 43210 USA
[3] Univ Kansas, Med Ctr, Dept Neurol, 3901 Rainbow Blvd,MS 2012, Kansas City, KS 66160 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Physiol, Los Angeles, CA 90095 USA
[5] Sorbonne Univ, Univ Hosp Pitie Salpetriere, AP HP, INSERM,Serv Neuromyol, Paris, France
[6] Univ Hosp Pitie Salpetriere, Inst Myol, UMR 974, Paris, France
[7] Univ Rochester, Dept Neurol, Rochester, NY USA
[8] UCL, Queen Sq Inst Neurol, MRC Ctr Neuromuscular Dis, Dept Neuromuscular Dis, London, England
[9] Casa Cura Policlin, Dept Neurorehabil Sci, Milan, Italy
[10] Univ Milan, Dept Biomed Sci Hlth, Milan, Italy
[11] Univ Milan, Neurorehabil Unit, NEuroMuscular Omnictr NEMO, Fdn Serena Onlus, Milan, Italy
[12] UT Southwestern Med Ctr, Dept Neurol & Neurotherapeut, Dallas, TX USA
关键词
management; myotonia congenita; nondystrophic myotonias; paramyotonia congenita; skeletal muscle channelopathies; MUSCLE CHLORIDE CHANNEL; SKELETAL-MUSCLE; PARAMYOTONIA-CONGENITA; ELECTRICAL MYOTONIA; DYSTROPHY TYPE-2; INTERCOSTAL MUSCLE; CLCN1; MUTATIONS; ALPHA-SUBUNIT; EXERCISE TEST; ION CHANNELS;
D O I
10.1002/mus.26887
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The nondystrophic myotonias are rare muscle hyperexcitability disorders caused by gain-of-function mutations in the SCN4A gene or loss-of-function mutations in the CLCN1 gene. Clinically, they are characterized by myotonia, defined as delayed muscle relaxation after voluntary contraction, which leads to symptoms of muscle stiffness, pain, fatigue, and weakness. Diagnosis is based on history and examination findings, the presence of electrical myotonia on electromyography, and genetic confirmation. In the absence of genetic confirmation, the diagnosis is supported by detailed electrophysiological testing, exclusion of other related disorders, and analysis of a variant of uncertain significance if present. Symptomatic treatment with a sodium channel blocker, such as mexiletine, is usually the first step in management, as well as educating patients about potential anesthetic complications.
引用
收藏
页码:430 / 444
页数:15
相关论文
共 50 条
  • [1] The nondystrophic myotonias
    Chad R. Heatwole
    Richard T. Moxley
    [J]. Neurotherapeutics, 2007, 4 : 238 - 251
  • [2] The nondystrophic Myotonias
    Heatwole, Chad R.
    Moxey, Richard T., III
    [J]. NEUROTHERAPEUTICS, 2007, 4 (02) : 238 - 251
  • [3] The familial periodic paralyses and nondystrophic myotonias
    Ptácek, L
    [J]. AMERICAN JOURNAL OF MEDICINE, 1998, 105 (01): : 58 - 70
  • [4] HEREDITARY NONDYSTROPHIC MYOTONIAS AND PERIODIC PARALYZES
    LEHMANNHORN, F
    RUDEL, R
    [J]. CURRENT OPINION IN NEUROLOGY, 1995, 8 (05) : 402 - 410
  • [5] THE COURSE AND OUTCOME OF PREGNANCY IN WOMEN WITH NONDYSTROPHIC MYOTONIAS
    Snyder, Yuliya
    Donlin-Smith, Colleen
    Snyder, Eric
    Pressman, Eva
    Ciafaloni, Emma
    [J]. MUSCLE & NERVE, 2015, 52 (06) : 1013 - 1015
  • [6] EVIDENCE OF GENETIC-HETEROGENEITY AMONG THE NONDYSTROPHIC MYOTONIAS
    PTACEK, LJ
    ZITER, FA
    ROBERTS, JW
    LEPPERT, MF
    [J]. NEUROLOGY, 1992, 42 (05) : 1046 - 1048
  • [7] Skeletal muscle channelopathies: nondystrophic myotonias and periodic paralysis
    Rayan, Dipa L. Raja
    Hanna, Michael G.
    [J]. CURRENT OPINION IN NEUROLOGY, 2010, 23 (05) : 466 - 476
  • [8] The nondystrophic myotonias: Genotype-phenotype correlation and longitudinal study. Clinical phenotype characterization
    Walsh, Ronan
    Wang, Yunxia
    Statland, Jeffery M.
    Bundy, Brain
    Barohn, Richard J.
    [J]. NEUROLOGY, 2007, 68 (12) : A297 - A297
  • [9] Skeletal-muscle channelopathies: periodic paralysis and nondystrophic myotonias
    Ryan, Aisling M.
    Matthews, Emma
    Hanna, Michael G.
    [J]. CURRENT OPINION IN NEUROLOGY, 2007, 20 (05) : 558 - 563
  • [10] Spectrum of sodium channel disturbances in the nondystrophic myotonias and periodic paralyses
    Cannon, SC
    [J]. KIDNEY INTERNATIONAL, 2000, 57 (03) : 772 - 779