Acoustic Analysis of Phonation in Children With Smith–Magenis Syndrome

dc.contributor.authorHidalgo-De la Guía, Irene
dc.contributor.authorGarayzábal-Heinze, Elena
dc.contributor.authorGómez-Vilda, Pedro
dc.contributor.authorMartínez-Olalla, Rafael
dc.contributor.authorPalacios-Alonso, Daniel
dc.date.accessioned2026-05-11T13:22:47Z
dc.date.issued2021-06-03
dc.description.abstractComplex simultaneous neuropsychophysiological mechanisms are responsible for the processing of the information to be transmitted and for the neuromotor planning of the articulatory organs involved in speech. The nature of this set of mechanisms is closely linked to the clinical state of the subject. Thus, for example, in populations with neurodevelopmental deficits, these underlying neuropsychophysiological procedures are deficient and determine their phonation. Most of these cases with neurodevelopmental deficits are due to a genetic abnormality, as is the case in the population with Smith–Magenis syndrome (SMS). SMS is associated with neurodevelopmental deficits, intellectual disability, and a cohort of characteristic phenotypic features, including voice quality, which does not seem to be in line with the gender, age, and complexion of the diagnosed subject. The phonatory profile and speech features in this syndrome are dysphonia, high f0, excess vocal muscle stiffness, fluency alterations, numerous syllabic simplifications, phoneme omissions, and unintelligibility of speech. This exploratory study investigates whether the neuromotor deficits in children with SMS adversely affect phonation as compared to typically developing children without neuromotor deficits, which has not been previously determined. The authors compare the phonatory performance of a group of children with SMS (N = 12) with a healthy control group of children (N = 12) matched in age, gender, and grouped into two age ranges. The first group ranges from 5 to 7 years old, and the second group goes from 8 to 12 years old. Group differences were determined for two forms of acoustic analysis performed on repeated recordings of the sustained vowel /a/ F1 and F2 extraction and cepstral peak prominence (CPP). It is expected that the results will enlighten the question of the underlying neuromotor aspects of phonation in SMS population. These findings could provide evidence of the susceptibility of phonation of speech to neuromotor disturbances, regardless of their origin.
dc.identifier.citationHidalgo-De la Guía I, Garayzábal-Heinze E, Gómez-Vilda P, Martínez-Olalla R and Palacios-Alonso D (2021) Acoustic Analysis of Phonation in Children With Smith–Magenis Syndrome. Front. Hum. Neurosci. 15:661392. doi: 10.3389/fnhum.2021.661392
dc.identifier.doihttps://doi.org/10.3389/fnhum.2021.661392
dc.identifier.issneISSN 1662-5161
dc.identifier.publicationfirstpage1
dc.identifier.publicationlastpage15
dc.identifier.publicationtitleFrontiers in Human Neuroscience
dc.identifier.publicationvolume15
dc.identifier.urihttps://hdl.handle.net/10115/204617
dc.language.isoen
dc.publisherFrontiers Media SA
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectSmith–Magenis
dc.subjectSyndrome
dc.subjectSpeech
dc.subjectCepstral peak prominence
dc.subjectPhonation stability
dc.subjectChildren
dc.titleAcoustic Analysis of Phonation in Children With Smith–Magenis Syndrome
dc.typeArticle
dc.type.hasVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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