Surgical correction of hyperlordosis in facioscapulohumeral muscular dystrophy: A case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery
Link
http://link.springer.com/content/pdf/10.1186/s12893-017-0276-0.pdf
Reference9 articles.
1. Evangelista T, Wood L, Fernandez-Torron R, Williams M, Smith D, Lunt P, et al. Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry. J Neurol. 2016;263(7):1401–8.
2. Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, et al. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nat Genet. 1992;2(1):26–30.
3. Lemmers RJ, Tawil R, Petek LM, Balog J, Block GJ, Santen GW, et al. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2. Nat Genet. 2012;44(12):1370–4.
4. Andersen G, Prahm KP, Dahlqvist JR, Citirak G, Vissing J. Aerobic training and postexercise protein in facioscapulohumeral muscular dystrophy: RCT study. NEUROLOGY. 2015;85(5):396–403.
5. Lee CS, Kang SJ, Hwang CJ, Lee SW, Ahn YJ, Kim YT, et al. Early-onset facioscapulohumeral muscular dystrophy - significance of pelvic extensors in sagittal spinal imbalance. J PEDIATR ORTHOP B. 2009;18(6):325–9.
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3. Staged Management of Cervicothoracic Lordosis and Scoliosis in an Emery-Dreifuss VI Muscular Dystrophy Patient;JBJS Case Connector;2021
4. Letter to the Editor Regarding “Non-Union After Multiple Lumbar Fusion Surgeries in a Patient with Facioscapulohumeral Muscular Dystrophy: A Case Report”;World Neurosurgery;2020-09
5. Spinal fusion in facioscapulohumeral dystrophy for hyperlordosis;Medicine;2020-02
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