Orofacial dysfunction in children and adolescents with myotonic dystrophy.

• Myotonic dystrophy (DM) is a neuromuscular disorder caused by an expansion of a CTG repeat sequence on chromosome 19q13. The aim of the present study was to describe the characteristics and prevalence of oral motor dysfunction in a cohort of children and adolescents with DM and to correlate different aspects of oral motor function with the type of DM and sex. Fifty-six individuals with DM (30 males, 26 females; median age 13y 2mo; range 2y 6mo-21y 5mo) were compared with healthy controls. They were divided into four subgroups: severe congenital DM (n=18); mild congenital DM (n=18); childhood DM (n=18); and classical DM (n=2). A speech-language pathologist assessed different variables of oral motor function, intelligibility, and lip force. The families used a questionnaire to report on eating difficulties and drooling. All individuals with DM had impaired facial expression. Intelligibility was moderately or severely reduced in 30 patients (60%), excluding six patients without speech. Most had a moderate or severe impairment of lip motility (76.0%), tongue motility (52.2%), and lip force (69.2%), causing deviant production of bilabial and dental consonants. The families reported problems with eating (51.9%) and drooling (37.0%). Oral motor dysfunction was most prominent in congenital DM, and males were more affected than females.

Nyckelord

Adolescent

Articulation Disorders

diagnosis

epidemiology

physiopathology

Child

Child

Preschool

Cohort Studies

Cross-Sectional Studies

Dyskinesia

Drug-Induced

diagnosis

epidemiology

physiopathology

Female

Humans

Lip

physiopathology

Male

Myotonic Dystrophy

epidemiology

genetics

Observer Variation

Parents

Phonetics

Prevalence

Severity of Illness Index

Sex Distribution

Publikations- och innehållstyp

ref (ämneskategori)

art (ämneskategori)