Orofacial dysfunction in Duchenne muscular dystrophy.

Détails

ID Serval
serval:BIB_7C1350B4748E
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Orofacial dysfunction in Duchenne muscular dystrophy.
Périodique
Archives of Oral Biology
Auteur⸱e⸱s
Botteron S., Verdebout C.M., Jeannet P.Y., Kiliaridis S.
ISSN
1879-1506[electronic]
Statut éditorial
Publié
Date de publication
2009
Volume
54
Numéro
1
Pages
26-31
Langue
anglais
Résumé
Duchenne muscular dystrophy (DMD) affects orofacial function. Our aim was to evaluate certain characteristics of orofacial function in DMD and relate possible deteriorations to the age of the patients and to the diminished internal structure quality of the masseter muscle. Bite force and finger force were measured in 16 DMD patients (6-20 years old) and 16 age matched controls. The thickness and internal structure quality of the masseter muscle were evaluated ultrasonographically. We found reduced mouth opening but no signs of masticatory muscle tenderness. Bite force values were lower for DMD patients. Masseter thickness showed no significant differences between the two groups, but poorer internal muscle structure quality characterised the elder, non-walking DMD patients explaining their low bite force values. In conclusion, the masseter muscle follows the general progress of the disease. Orofacial function in DMD patients is becoming ever more important as their life expectancy increases.
Mots-clé
Adolescent, Age Factors, Bite Force, Child, Disease Progression, Female, Humans, Male, Masseter Muscle/physiopathology, Masseter Muscle/ultrasonography, Muscular Dystrophy, Duchenne/physiopathology, Muscular Dystrophy, Duchenne/ultrasonography, Young Adult
Pubmed
Web of science
Création de la notice
04/01/2010 18:03
Dernière modification de la notice
20/08/2019 15:37
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