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
  • [1] Survival of patients with Duchenne muscular dystrophy
    San Martin P, Pamela
    Solis F, Fresia
    Cavada Ch, Gabriel
    REVISTA CHILENA DE PEDIATRIA-CHILE, 2018, 89 (04): : 477 - 483
  • [2] Autophagy as a new therapeutic target in Duchenne muscular dystrophy
    C De Palma
    F Morisi
    S Cheli
    S Pambianco
    V Cappello
    M Vezzoli
    P Rovere-Querini
    M Moggio
    M Ripolone
    M Francolini
    M Sandri
    E Clementi
    Cell Death & Disease, 2012, 3 : e418 - e418
  • [3] Autophagy as a new therapeutic target in Duchenne muscular dystrophy
    De Palma, C.
    Morisi, F.
    Cheli, S.
    Pambianco, S.
    Cappello, V.
    Vezzoli, M.
    Rovere-Querini, P.
    Moggio, M.
    Ripolone, M.
    Francolini, M.
    Sandri, M.
    Clementi, E.
    CELL DEATH & DISEASE, 2012, 3 : e418 - e418
  • [4] Impact of Bisphosphonates on Survival for Patients With Duchenne Muscular Dystrophy
    Gordon, Kevin E.
    Dooley, Joseph M.
    Sheppard, Kayla M.
    MacSween, Judith
    Esser, Michael J.
    PEDIATRICS, 2011, 127 (02) : E353 - E358
  • [5] Cardiac phenotype determines survival in Duchenne muscular dystrophy
    Birnkrant, David J.
    Ararat, Erhan
    Mhanna, Maroun J.
    PEDIATRIC PULMONOLOGY, 2016, 51 (01) : 70 - 76
  • [6] Forty-Eight Years with Duchenne Muscular Dystrophy
    Bach, John Robert
    DeCicco, Anthony
    AMERICAN JOURNAL OF PHYSICAL MEDICINE & REHABILITATION, 2011, 90 (10) : 868 - 870
  • [7] Cough augmentation in Duchenne muscular dystrophy
    Ishikawa, Yuka
    Bach, John R.
    Komaroff, Eugene
    Miura, Toshihiko
    Jackson-Parekh, Roseanna
    AMERICAN JOURNAL OF PHYSICAL MEDICINE & REHABILITATION, 2008, 87 (09) : 726 - 730
  • [8] Duchenne muscular dystrophy
    Yiu, Eppie M.
    Kornberg, Andrew J.
    NEUROLOGY INDIA, 2008, 56 (03) : 236 - 247
  • [9] Duchenne muscular dystrophy
    Susan T. Iannaccone
    Zohair Nanjiani
    Current Treatment Options in Neurology, 2001, 3 (2) : 105 - 117
  • [10] Duchenne muscular dystrophy
    Yiu, Eppie M.
    Kornberg, Andrew J.
    JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2015, 51 (08) : 759 - 764