Late-onset myopathy of the posterior calf muscles mimicking Miyoshi myopathy unrelated to dysferlin mutation: a case report

被引：6
|
作者：
Clemens Neusch
Tanja Kuhlmann
Wolfram Kress
Christiane Schneider-Gold
机构：
[1] University of Ulm,Department of Neurology
[2] University Hospital Münster,Institute of Neuropathology
[3] University of Würzburg,Institute of Human Genetics
[4] Biozentrum,Department of Neurology
[5] University of Bochum,undefined
[6] St Josef Hospital,undefined
来源：
Journal of Medical Case Reports | / 6卷 / 1期
关键词：
Myopathy; Gastrocnemius Muscle; Calf Muscle; Compound Muscle Action Potential Amplitude; Distal Myopathy;
D O I：
10.1186/1752-1947-6-345
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [21] Late-onset polyglucosan body myopathy in five patients with a homozygous mutation in GYG1
    Akman, H. Orhan
    Aykit, Yavuz
    Amuk, Ozge Ceren
    Malfatti, Edoardo
    Romero, Norma B.
    Maioli, Maria Antonietta
    Piras, Rachele
    DiMauro, Salvatore
    Marrosu, Gianni
    NEUROMUSCULAR DISORDERS, 2016, 26 (01) : 16 - 20
  • [22] Late-onset distal myopathy affecting posterior calves - serial MRI showing sequential muscle involvement
    Lamont, Phillipa J.
    Leong, Wai
    Fabian, Vicki
    Laing, Nigel G.
    NEUROMUSCULAR DISORDERS, 2006, 16 : S92 - S93
  • [23] A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNATrp gene
    Silvestri, G
    Rana, M
    DiMuzio, A
    Uncini, A
    Tonali, P
    Servidei, S
    NEUROMUSCULAR DISORDERS, 1998, 8 (05) : 291 - 295
  • [24] Novel GYG1 mutation causing late-onset polyglucosan body myopathy with nemaline rods
    Tasca, G.
    Fattori, F.
    Monforte, M.
    Hedberg-Oldfors, C.
    Sabatelli, M.
    Udd, B.
    Boldrini, R.
    Bertini, E.
    Ricci, E.
    Oldfors, A.
    NEUROMUSCULAR DISORDERS, 2016, 26 : S199 - S200
  • [25] A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy
    Maeso, E.
    Rueda, A.
    Jimenez, S.
    del Hoyo, P.
    Martin, R.
    Cabello, A.
    Mendoza, L. M.
    Arenas, J.
    Campos, Y.
    NEUROMUSCULAR DISORDERS, 2007, 17 (05) : 415 - 418
  • [26] Novel GYG1 mutation causing late-onset polyglucosan body myopathy with nemaline rods
    Tasca, G.
    Fattori, F.
    Monforte, M.
    Hedberg-Oldfors, C.
    Sabatelli, M.
    Udd, B.
    Bertini, E.
    Ricci, E.
    Oldfors, A.
    EUROPEAN JOURNAL OF NEUROLOGY, 2016, 23 : 827 - 827
  • [27] A novel dynamin-2 gene mutation associated with a late-onset centronuclear myopathy with necklace fibres
    Casar-Borota, Olivera
    Jacobsson, Johan
    Libelius, Rolf
    Oldfors, Carola Hedberg
    Malfatti, Edoardo
    Romero, Norma Beatriz
    Oldfors, Anders
    NEUROMUSCULAR DISORDERS, 2015, 25 (04) : 345 - 348
  • [28] Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patients
    Okhovat, Ali Asghar
    Nilipour, Yalda
    Boostani, Reza
    Vahabizad, Fahimeh
    Najmi, Safa
    Nafissi, Shahriar
    Fatehi, Farzad
    NEUROMUSCULAR DISORDERS, 2021, 31 (01) : 29 - 34
  • [29] Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case report
    Matthias Türk
    Armin M. Nagel
    Frank Roemer
    Ursula Schlötzer-Schrehardt
    Christian T. Thiel
    Martin Winterholler
    Rolf Schröder
    BMC Musculoskeletal Disorders, 20
  • [30] Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case report
    Tuerk, Matthias
    Nagel, Armin M.
    Roemer, Frank
    Schloetzer-Schrehardt, Ursula
    Thiel, Christian T.
    Winterholler, Martin
    Schroeder, Rolf
    BMC MUSCULOSKELETAL DISORDERS, 2019, 20 (01)
12345