Prednisone therapy in Becker's muscular dystrophy

被引:7
|
作者
Johnsen, SD [1 ]
机构
[1] Baylor Coll Med, Sect Child Neurol, Dept Pediat, Blue Bird Clin, Houston, TX 77030 USA
关键词
D O I
10.1177/08830738010160111406
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Two boys with Becker's muscular dystrophy had a dramatic and sustained improvement in strength with therapeutic use of prednisone. Both had documented Xp-21 defects on DNA testing. Concurrently with improvement, there was a decrease in their serum creatine kinase levels. One patient had two muscle biopsies, the first before prednisone treatment and the second during treatment. Both biopsies demonstrated an immunoblot decrease in the quantity of muscle dystrophin. Routine histology on the first biopsy was consistent with muscle dystrophy, and the second biopsy was normal. These two patients suggest that a small percentage of patients with Becker's muscular dystrophy have a dramatic and sustained improvement in strength with the use of therapeutic corticosteroids. All patients with Becker's muscular dystrophy should be given a careful trial of prednisone to define those who benefit.
引用
收藏
页码:870 / 871
页数:2
相关论文
共 50 条
  • [31] Left ventricular function and perfusion in Becker's muscular dystrophy
    Mansi, L
    Pace, L
    Politano, L
    Rambaldi, PF
    DiGregorio, F
    Raia, P
    Petretta, VR
    Nigro, G
    JOURNAL OF NUCLEAR MEDICINE, 1997, 38 (04) : 563 - 567
  • [32] Electroretinogram in Duchenne/Becker muscular dystrophy
    Pascual, SIP
    Molano, J
    Pascual-Castroviejo, I
    PEDIATRIC NEUROLOGY, 1998, 18 (04) : 315 - 320
  • [33] Utrophin assay in Becker muscular dystrophy
    Keyhani, Elahe
    Kahrizi, Kimia
    Shafeghati, Yousef
    banan, Mehdi
    Darabi, Elham
    Gharesouran, Jalal
    Najmabadi, Hossein
    VIRCHOWS ARCHIV, 2008, 452 : S124 - S124
  • [34] Epidemiology of Becker muscular dystrophy in the Netherlands
    Schrama, E.
    Koeks, Z.
    van de Velde, N.
    Kan, H.
    Krom, Y.
    van Duyvenvoorde, H.
    Niks, E.
    NEUROMUSCULAR DISORDERS, 2021, 31 : S88 - S89
  • [35] Duchenne/Becker muscular dystrophy: From molecular diagnosis to gene therapy
    Matsuo, M
    BRAIN & DEVELOPMENT, 1996, 18 (03): : 167 - 172
  • [36] Duchenne or Becker muscular dystrophy in girls
    Lescaut, W
    Butori, C
    Soriani, MH
    Desnuelles, C
    REVUE DE MEDECINE INTERNE, 2004, 25 (06): : 464 - 467
  • [37] Detrusor overactivity in becker muscular dystrophy
    Smith, Matthew D.
    Seth, Jai H.
    Hanna, Michael G.
    Panicker, Jalesh N.
    MUSCLE & NERVE, 2013, 47 (03) : 464 - 465
  • [38] Cardiac involvement in Becker muscular dystrophy
    Finsterer, Josef
    Stoellberger, Claudia
    CANADIAN JOURNAL OF CARDIOLOGY, 2008, 24 (10) : 786 - 792
  • [39] Cardiomyopathy in becker muscular dystrophy: Overview
    Ho, Rady
    Nguyen, My-Le
    Mather, Paul
    WORLD JOURNAL OF CARDIOLOGY, 2016, 8 (06): : 356 - 361
  • [40] Muscle MRI in Becker muscular dystrophy
    Iannaccone, E.
    Monforte, M.
    Tasca, G.
    Masciullo, M.
    Frusciante, R.
    Erra, C.
    Renna, R.
    Pelliccioni, M.
    Ottaviani, P.
    Laschena, F.
    Ricci, E.
    JOURNAL OF NEUROLOGY, 2011, 258 : 250 - 251