Literature DB >> 24646504

Temporalis muscle hypertrophy and reduced skull eccentricity in Duchenne muscular dystrophy.

C S M Straathof1, N Doorenweerd2, B H A Wokke3, E M Dumas3, J C van den Bergen3, M A van Buchem2, J G M Hendriksen4, J J G M Verschuuren3, H E Kan2.   

Abstract

Muscle hypertrophy and muscle weakness are well known in Duchenne muscular dystrophy. Decreased muscle force can have secondary effects on skeletal growth and development such as facial and dental morphology changes. In this study, we quantified temporal muscle thickness, circumference, and eccentricity of the skull and the head on T1-weighted magnetic resonance imaging (MRI) scans of the head of 15 Duchenne muscular dystrophy patients and 15 controls. Average temporal muscle thickness was significantly increased in patients (12.9 ± 5.2 mm) compared to controls (6.8 ± 1.4 mm) (P < .0001), whereas the shape of the skull was significantly rounder compared to controls. Temporal muscle thickness and skull eccentricity were significantly negatively correlated in patients, and positively in controls. Hypertrophy of the temporal muscles and changes in skull eccentricity appear to occur early in the course of Duchenne muscular dystrophy. Further studies in younger patients are needed to confirm a causal relationship.
© The Author(s) 2014.

Entities:  

Keywords:  MRI; muscle disease; muscular dystrophy; pediatric

Mesh:

Year:  2014        PMID: 24646504     DOI: 10.1177/0883073813518106

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  7 in total

Review 1.  Interventions for dysphagia in long-term, progressive muscle disease.

Authors:  Katherine Jones; Robert D S Pitceathly; Michael R Rose; Susan McGowan; Marguerite Hill; Umesh A Badrising; Tom Hughes
Journal:  Cochrane Database Syst Rev       Date:  2016-02-09

2.  Cognitive impairment appears progressive in the mdx mouse.

Authors:  Emine Bagdatlioglu; Paola Porcari; Elizabeth Greally; Andrew M Blamire; Volker W Straub
Journal:  Neuromuscul Disord       Date:  2020-03-04       Impact factor: 4.296

3.  Orofacial muscles may be affected in early stages of Becker muscular dystrophy: A preliminary study.

Authors:  Marloes L J Lagarde; Nens van Alfen; Alexander C H Geurts; Imelda J M de Groot; Lenie van den Engel-Hoek
Journal:  Muscle Nerve       Date:  2019-12-24       Impact factor: 3.217

Review 4.  Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review.

Authors:  Jagath C Ranasinghe; Chandani Wickramasinghe; Ganganath Rodrigo
Journal:  BMC Pediatr       Date:  2018-02-19       Impact factor: 2.125

5.  Influence of full-length dystrophin on brain volumes in mouse models of Duchenne muscular dystrophy.

Authors:  Bauke Kogelman; Artem Khmelinskii; Ingrid Verhaart; Laura van Vliet; Diewertje I Bink; Annemieke Aartsma-Rus; Maaike van Putten; Louise van der Weerd
Journal:  PLoS One       Date:  2018-03-30       Impact factor: 3.240

Review 6.  Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy.

Authors:  Michael Naidoo; Karen Anthony
Journal:  Mol Neurobiol       Date:  2019-12-13       Impact factor: 5.590

7.  Decision-Making And Selection Bias in Four Observational Studies on Duchenne and Becker Muscular Dystrophy.

Authors:  Karin J Naarding; Nathalie Doorenweerd; Zaïda Koeks; Ruben G F Hendriksen; Kinita A Chotkan; Yvonne D Krom; Imelda J M de Groot; Chiara S Straathof; Erik H Niks; Hermien E Kan
Journal:  J Neuromuscul Dis       Date:  2020
  7 in total

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