Distal Myopathies

被引:8
|
作者
Felice, Kevin J. [1 ,2 ,3 ]
机构
[1] Hosp Special Care, Charles H Kaman Fdn Neuromuscular, 2150 Corbin Ave, New Britain, CT 06053 USA
[2] Hosp Special Care, Muscular Dystrophy Assoc Care Ctr, 2150 Corbin Ave, New Britain, CT 06053 USA
[3] Univ Connecticut, Sch Med, Farmington, CT USA
关键词
Distal myopathy; Myofibrillar myopathy; Congenital myopathy; Muscular dystrophy; Genetic myopathy; MUSCULAR-DYSTROPHY FSHD; MUTATIONS; SKELETAL; GENE; DIAGNOSIS; DYSFERLIN; MYOSITIS; LINKAGE;
D O I
10.1016/j.ncl.2020.03.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The distal myopathies are a rare and heterogeneous group of neuromuscular disorders. Patients present with weakness of the hands, distal lower extremities, or both. Age of onset varies from early childhood to late adulthood. Most of the disorders causing distal myopathic weakness are genetically based. The list of genetic disorders associated with distal-onset weakness is ever-expanding and complicated by pronounced genetic heterogeneity, phenotypic variability, and complex multisystem involvement. There are no known effective disease-modifying treatments for the distal myopathies. Evaluation, symptomatic management, and periodic monitoring of patients in a multidisciplinary neuromuscular center are the mainstays of care. © 2020 Elsevier Inc.
引用
收藏
页码:637 / 659
页数:23
相关论文
共 50 条
  • [21] Myosin myopathies and distal arthrogryposis syndromes
    Oldfors, A.
    Tajsharghi, H.
    Kimber, E.
    Darin, N.
    Lindberg, C.
    NEUROMUSCULAR DISORDERS, 2010, 20 (9-10) : 635 - 635
  • [22] Diagnostic value of NGS in distal myopathies
    Marti, P.
    Muelas, N.
    Azorin, I.
    Casasus, A.
    Vilchez, R.
    Vilchez, J. J.
    EUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 : 354 - 354
  • [23] The unfolding spectrum of inherited distal myopathies
    Milone, Margherita
    Liewluck, Teerin
    MUSCLE & NERVE, 2019, 59 (03) : 283 - 294
  • [24] MRI PATTERN IN THE WORKUP OF DISTAL MYOPATHIES
    Bugiardini, E.
    Morrow, J. M.
    Shah, S.
    Parton, M. J.
    Yousry, T. A.
    Hanna, M. G.
    MUSCLE & NERVE, 2015, 52 : S2 - S2
  • [25] Clinical and genetic aspects of distal myopathies
    Saperstein, DS
    Amato, AA
    Barohn, RJ
    MUSCLE & NERVE, 2001, 24 (11) : 1440 - 1450
  • [26] Clinical and genetic characterization of distal myopathies
    Cabrera, M.
    Junckerstorff, R.
    Needham, M.
    Lamont, P. J.
    Laing, N. G.
    NEUROMUSCULAR DISORDERS, 2014, 24 (9-10) : 810 - 810
  • [27] Distal Myopathies: A Retrospective Study of 28 Cases
    Franques, Jerome
    Campana-Salort, Emmanuelle
    Attarian, Shahram
    Verschueren, Annie
    Eymard, Bruno
    Fernandez, Carla
    De Paula, Andre Maues
    Figarella-Branger, Dominique
    Levy, Nicolas
    Richard, Pascale
    Monnier, Nicole
    Wallgren-Pettersson, Carina
    Udd, Bjarne
    Pellissier, Jean-Francois
    Pouget, Jean
    NEUROLOGY, 2010, 74 (09) : A516 - A516
  • [28] Overview of distal myopathies: from the clinical to the molecular
    Barohn, RJ
    Amato, AA
    Griggs, RC
    NEUROMUSCULAR DISORDERS, 1998, 8 (05) : 309 - 316
  • [29] Distal myopathies: clinical and molecular diagnosis and classification
    Mastaglia, FL
    Laing, NG
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 67 (06): : 703 - 707
  • [30] Retrospective study of 29 cases of distal myopathies
    Franques, J.
    Campana-Salort, E.
    Attarian, S.
    Verschueren, A.
    Fernandez, C.
    de Paula, A. Maues
    Figarella-Branger, D.
    Pouget, J.
    NEUROMUSCULAR DISORDERS, 2009, 19 (8-9) : 567 - 568