Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Sep;2(3):185-194.
doi: 10.21037/jss.2016.08.05.

Duchenne muscular dystrophy: the management of scoliosis

Affiliations
Review

Duchenne muscular dystrophy: the management of scoliosis

James E Archer et al. J Spine Surg. 2016 Sep.

Abstract

This study summaries the current management of scoliosis in patients with Duchenne Muscular Dystrophy. A literature review of Medline was performed and the collected articles critically appraised. This literature is discussed to give an overview of the current management of scoliosis within Duchenne Muscular Dystrophy. Importantly, improvements in respiratory care, the use of steroids and improving surgical techniques have allowed patients to maintain quality of life and improved life expectancy in this patient group.

Keywords: Duchenne muscular dystrophy; scoliosis; spinal surgery.

PubMed Disclaimer

Conflict of interest statement

The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Radiographs demonstrating the difference in curve pattern between that seen in Adolescent Idiopathic Scoliosis and Duchenne Muscular Dystrophy Scoliosis. (A) An anteroposterior radiograph of a patient with adolescent idiopathic scoliosis; (B) shows an anteroposterior radiograph of a DMD patient with scoliosis demonstrating the difference in curve pattern and location within the spine.
Figure 2
Figure 2
A post-operative anteroposterior radiograph of the earlier DMD patient after surgical instrumentation with fusion to the pelvis. The proximal extent of the instrumentation and fusion is T2, however, this patient had already lost the ability to self-feed.

Similar articles

Cited by

References

    1. Bushby K. Duchenne muscular dystrophy factsheet.pdf. Muscular Dystrophy Campaign; 2012.
    1. Hoffman EP, Brown RH, Jr, Kunkel LM. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 1987;51:919-28. 10.1016/0092-8674(87)90579-4 - DOI - PubMed
    1. van Ruiten HJ, Straub V, Bushby K, et al. Improving recognition of Duchenne muscular dystrophy: a retrospective case note review. Arch Dis Child 2014;99:1074-7. 10.1136/archdischild-2014-306366 - DOI - PMC - PubMed
    1. Bushby KM, Hill A, Steele JG. Failure of early diagnosis in symptomatic Duchenne muscular dystrophy. Lancet 1999;353:557-8. 10.1016/S0140-6736(98)05279-9 - DOI - PubMed
    1. Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol 2010;9:77-93. 10.1016/S1474-4422(09)70271-6 - DOI - PubMed

LinkOut - more resources