Assessment of Dysphonia in Children with Pompe Disease Using Auditory-Perceptual and Acoustic/Physiologic Methods.
Abstract
Bulbar and respiratory weakness occur commonly in children with Pompe disease and
frequently lead to dysarthria. However, changes in vocal quality associated with this
motor speech disorder are poorly described. The goal of this study was to characterize
the vocal function of children with Pompe disease using auditory-perceptual and physiologic/acoustic
methods. High-quality voice recordings were collected from 21 children with Pompe
disease. The Grade, Roughness, Breathiness, Asthenia, and Strain (GRBAS) scale was
used to assess voice quality and ratings were compared to physiologic/acoustic measurements
collected during sustained phonation tasks, reading of a standard passage, and repetition
of a short phrase at maximal volume. Based on ratings of grade, dysphonia was present
in 90% of participants and was most commonly rated as mild or moderate in severity.
Duration of sustained phonation tasks was reduced and shimmer was increased in comparison
to published reference values for children without dysphonia. Specific measures of
loudness were found to have statistically significant relationships with perceptual
ratings of grade, breathiness, asthenia, and strain. Our data suggest that dysphonia
is common in children with Pompe disease and primarily reflects impairments in respiratory
and laryngeal function; however, the primary cause of dysphonia remains unclear. Future
studies should seek to quantify the relative contribution of deficits in individual
speech subsystems on voice quality and motor speech performance more broadly.
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https://hdl.handle.net/10161/24019Published Version (Please cite this version)
10.3390/jcm10163617Publication Info
Crisp, Kelly D; Neel, Amy T; Amarasekara, Sathya; Marcus, Jill; Nichting, Gretchen;
Korlimarla, Aditi; ... Jones, Harrison N (2021). Assessment of Dysphonia in Children with Pompe Disease Using Auditory-Perceptual and
Acoustic/Physiologic Methods. Journal of clinical medicine, 10(16). pp. 3617-3617. 10.3390/jcm10163617. Retrieved from https://hdl.handle.net/10161/24019.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Harrison N. Jones
Associate Professor of Head and Neck Surgery & Communication Sciences
Priya Sunil Kishnani
Chen Family Distinguished Professor of Pediatrics
RESEARCH INTERESTS A multidisciplinary approach to care of individuals with genetic
disorders in conjunction with clinical and bench research that contributes to: 1)
An understanding of the natural history and delineation of long term complications
of genetic disorders with a special focus on liver Glycogen storage disorders, lysosomal
disorders with a special focus on Pompe disease, Down syndrome and hypophosphatasia2) )
The development of new therapies such
Aditi Korlimarla
Medical Instructor in the Department of Pediatrics
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