Literature DB >> 25096430

Duchenne muscular dystrophy.

Ellen J Annexstad1, Inger Lund-Petersen2, Magnhild Rasmussen3.   

Abstract

BACKGROUND: Duchenne muscular dystrophy is one of the most severe muscle diseases to affect children. In the last twenty years, treatments have been established that have significantly improved patients' quality of life and life expectancy. The purpose of this article is to outline the main features of the disease and its treatment, and to examine possible future treatment options.
METHOD: The article is based on a literature search in PubMed, current international guidelines and our own clinical experience.
RESULTS: Close monitoring by an interdisciplinary rehabilitation team forms the basis of treatment. Treatment with glucocorticoids can slow disease progression and improve motor function in the short term. The treatment may cause side effects, which must be monitored and which may require intervention. A not insignificant proportion of patients have cognitive and neuropsychiatric problems that must be addressed. Active intervention in response to signs of respiratory or cardiac failure is important. More causal treatment of Duchenne muscular dystrophy is under testing and offers cautious hope for future patients.
INTERPRETATION: With improved treatment and increased life expectancy come new challenges for patients with Duchenne muscular dystrophy and their families, as well as new demands on the support services. This patient group requires close and comprehensive follow-up, also in the transition from child to adult.

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Year:  2014        PMID: 25096430     DOI: 10.4045/tidsskr.13.0836

Source DB:  PubMed          Journal:  Tidsskr Nor Laegeforen        ISSN: 0029-2001


  7 in total

Review 1.  Skeletal muscle atrophy: disease-induced mechanisms may mask disuse atrophy.

Authors:  C J Malavaki; G K Sakkas; G I Mitrou; A Kalyva; I Stefanidis; K H Myburgh; C Karatzaferi
Journal:  J Muscle Res Cell Motil       Date:  2016-01-04       Impact factor: 2.698

Review 2.  Cardiac care of children with dystrophinopathy and females carrying DMD-gene variations.

Authors:  John Bourke; Cathy Turner; William Bradlow; Ashish Chikermane; Caroline Coats; Matthew Fenton; Maria Ilina; Alexandra Johnson; Stam Kapetanakis; Lisa Kuhwald; Adrian Morley-Davies; Ros Quinlivan; Konstantinos Savvatis; Marianela Schiava; Zaheer Yousef; Michela Guglieri
Journal:  Open Heart       Date:  2022-10

3.  Comparison of Experimental Protocols of Physical Exercise for mdx Mice and Duchenne Muscular Dystrophy Patients.

Authors:  Janek Hyzewicz; Urs T Ruegg; Shin'ichi Takeda
Journal:  J Neuromuscul Dis       Date:  2015-11-22

4.  Assessment of Weighted Gene Co-Expression Network Analysis to Explore Key Pathways and Novel Biomarkers in Muscular Dystrophy.

Authors:  Xiaoxue Xu; Yuehan Hao; Jiao Wu; Jing Zhao; Shuang Xiong
Journal:  Pharmgenomics Pers Med       Date:  2021-04-13

5.  Myosin Binding Protein-C Slow Phosphorylation is Altered in Duchenne Dystrophy and Arthrogryposis Myopathy in Fast-Twitch Skeletal Muscles.

Authors:  Maegen A Ackermann; Christopher W Ward; Christina Gurnett; Aikaterini Kontrogianni-Konstantopoulos
Journal:  Sci Rep       Date:  2015-08-19       Impact factor: 4.379

6.  Ratio of Creatine Kinase to Alanine Aminotransferase as a Biomarker of Acute Liver Injury in Dystrophinopathy.

Authors:  Liang Wang; Menglong Chen; Min Xu; Jing Li; Pinning Feng; Ruojie He; Yuling Zhu; Huan Li; Jinfu Lin; Cheng Zhang
Journal:  Dis Markers       Date:  2018-06-19       Impact factor: 3.434

7.  Flexible intramedullary nailing for supracondylar femoral fractures in children with Duchenne muscular dystrophy.

Authors:  Marco Distefano; Camilla Bettuzzi; Giada Salvatori; Giovanna Cristella; Caterina Novella Abati; Manuele Lampasi
Journal:  Am J Case Rep       Date:  2020-11-11
  7 in total

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