New Survival Target for Duchenne Muscular Dystrophy

被引:8
作者
Villanova, Marcello [1 ]
Kazibwe, Sifa [1 ]
机构
[1] Nigrisoli Hosp, Neuromuscular Rehabil Unit, Bologna, Italy
关键词
Duchenne Muscular Dystrophy; Neuromuscular Disease; Survival; Noninvasive Mechanical Ventilation; VENTILATORY SUPPORT;
D O I
10.1097/PHM.0000000000000569
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
We report a patient with a typical phenotype and clinical history of Duchenne muscular dystrophy who is currently 53 years old. Because of improvements in cardiopulmonary care, there has been a great improvement in survival and preservation of quality of life for many of these patients. Whereas it is no longer rare to find patients with Duchenne muscular dystrophy living into their fifth decade, this is the first report of a patient in his sixth decade of life. We believe that besides use of continuous noninvasive respiratory support, the fortuitous absence of dilated cardiomyopathy associated with the particular point mutation of his dystrophin gene has permitted prolonged survival.
引用
收藏
页码:E28 / E30
页数:3
相关论文
共 50 条
  • [31] Duchenne Muscular Dystrophy: Continuous Noninvasive Ventilatory Support Prolongs Survival
    Bach, John R.
    Martinez, Daniel
    RESPIRATORY CARE, 2011, 56 (06) : 744 - 750
  • [32] Cardiopulmonary phenotypic variability and discordance in Duchenne muscular dystrophy: Implications for new therapies
    Birnkrant, David J.
    Carter, John C.
    PEDIATRIC PULMONOLOGY, 2021, 56 (04) : 738 - 746
  • [33] A comparison of swallowing dysfunction in Becker muscular dystrophy and Duchenne muscular dystrophy
    Yamada, Yuka
    Kawakami, Michiyuki
    Wada, Ayako
    Otsuka, Tomoyoshi
    Muraoka, Kaori
    Liu, Meigen
    DISABILITY AND REHABILITATION, 2018, 40 (12) : 1421 - 1425
  • [34] Simvastatin offers new prospects for the treatment of Duchenne muscular dystrophy
    Whitehead, Nicholas P.
    Kim, Min Jeong
    Bible, Kenneth L.
    Adams, Marvin E.
    Froehner, Stanley C.
    RARE DISEASES, 2016, 4 (01)
  • [35] The effect of posterior spinal fusion on respiratory function in Duchenne muscular dystrophy
    Alexander, W. M.
    Smith, M.
    Freeman, B. J. C.
    Sutherland, L. M.
    Kennedy, J. D.
    Cundy, P. J.
    EUROPEAN SPINE JOURNAL, 2013, 22 (02) : 411 - 416
  • [36] Pharmacodynamic modelling of rocuronium in adolescents with Duchenne muscular dystrophy
    Ihmsen, Harald
    Viethen, Vanessa
    Forst, Juergen
    Schwilden, Helmut
    Schmitt, Hubert J.
    Muenster, Tino
    EUROPEAN JOURNAL OF ANAESTHESIOLOGY, 2009, 26 (02) : 105 - 110
  • [37] HEALTH PROFILE OF A COHORT OF ADULTS WITH DUCHENNE MUSCULAR DYSTROPHY
    Pandya, Shree
    James, Katherine A.
    Westfield, Christina
    Thomas, Shiny
    Fox, Deborah J.
    Ciafaloni, Emma
    Moxley, Richard T.
    MUSCLE & NERVE, 2018, 58 (02) : 219 - 223
  • [38] Duchenne Muscular Dystrophy Fatigue Trajectories
    Wei, Yi Sally
    Hnaini, Mona
    ElAloul, Basmah
    Zapata, Eugenio
    Campbell, Craig
    NEUROPEDIATRICS, 2024, 55 (01) : 42 - 48
  • [39] Update on the Treatment of Duchenne Muscular Dystrophy
    Rodino-Klapac, Louise R.
    Mendell, Jerry R.
    Sahenk, Zarife
    CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2013, 13 (03)
  • [40] Targeting Fibrosis in Duchenne Muscular Dystrophy
    Zhou, Lan
    Lu, Haiyan
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2010, 69 (08) : 771 - 776