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Dysarthria in hereditary spastic paraplegia type 4.
Jacinto-Scudeiro, Lais Alves; Rothe-Neves, Rui; Dos Santos, Vanessa Brzoskowski; Machado, Gustavo Dariva; Burguêz, Daniela; Padovani, Marina Martins Pereira; Ayres, Annelise; Rech, Rafaela Soares; González-Salazar, Carelis; Junior, Marcondes Cavalcante França; Saute, Jonas Alex Morales; Olchik, Maira Rozenfeld.
Afiliação
  • Jacinto-Scudeiro LA; Postgraduate Program in Medicine, Medical Sciences, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
  • Rothe-Neves R; Phonetics Laboratory of the Faculty of Letters, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • Dos Santos VB; Postgraduate Program in Medicine, Medical Sciences, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
  • Machado GD; Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
  • Burguêz D; Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
  • Padovani MMP; Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo, SP, Brazil.
  • Ayres A; Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.
  • Rech RS; Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.
  • González-Salazar C; Postgraduate Program in Medical Pathophysiology, Universidade Estadual de Campinas, São Paulo, SP, Brazil.
  • Junior MCF; Department of Neurology, Universidade Estadual de Campinas, São Paulo, SP, Brazil.
  • Saute JAM; Postgraduate Program in Medicine, Medical Sciences, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil; Internal Medicine Department, Faculdade de Medicina Universidade Federal do Rio Grande do
  • Olchik MR; Postgraduate Program in Medicine, Medical Sciences, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil; Department of Surgery and Orthopedics, Faculdade de Odontologia, Universidade Federal do
Clinics (Sao Paulo) ; 78: 100128, 2023.
Article em En | MEDLINE | ID: mdl-36473366
ABSTRACT

OBJECTIVE:

To describe the speech pattern of patients with hereditary Spastic Paraplegia type 4 (SPG4) and correlated it with their clinical data.

METHODS:

Cross-sectional study was carried out in two university hospitals in Brazil. Two groups participated in the study the case group (n = 28) with a confirmed genetic diagnosis for SPG4 and a control group (n = 17) matched for sex and age. The speech assessment of both groups included speech task recording, acoustic analysis, and auditory-perceptual analysis. In addition, disease severity was assessed with the Spastic Paraplegia Rating Scale (SPRS).

RESULTS:

In the auditory-perceptual analysis, 53.5% (n = 15) of individuals with SPG4 were dysarthric, with mild to moderate changes in the subsystems of phonation and articulation. On acoustic analysis, SPG4 subjects' performances were worse in measurements related to breathing (maximum phonation time) and articulation (speech rate, articulation rate). The articulation variables (speech rate, articulation rate) are related to the age of onset of the first motor symptom.

CONCLUSION:

Dysarthria in SPG4 is frequent and mild, and it did not evolve in conjunction with more advanced motor diseases. This data suggest that diagnosed patients should be screened and referred for speech therapy evaluation and those pathophysiological mechanisms of speech involvement may differ from the length-dependent degeneration of the corticospinal tract.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Tipo de estudo: Observational_studies Limite: Humans Idioma: En Revista: Clinics (Sao Paulo) Assunto da revista: MEDICINA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Tipo de estudo: Observational_studies Limite: Humans Idioma: En Revista: Clinics (Sao Paulo) Assunto da revista: MEDICINA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil
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