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Relevant bibliographies by topics / Orofacial apraxia / Journal articles

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Journal articles on the topic 'Orofacial apraxia'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Cera, Maysa Luchesi, Karin Zazo Ortiz, Paulo Henrique Ferreira Bertolucci, and Thaís Soares Cianciarullo Minett. "Speech and orofacial apraxias in Alzheimer's disease." International Psychogeriatrics 25, no. 10 (2013): 1679–85. http://dx.doi.org/10.1017/s1041610213000781.

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ABSTRACTBackground:Alzheimer's disease (AD) affects not only memory but also other cognitive functions, such as orientation, language, praxis, attention, visual perception, or executive function. Most studies on oral communication in AD focus on aphasia; however, speech and orofacial apraxias are also present in these patients. The aim of this study was to investigate the presence of speech and orofacial apraxias in patients with AD with the hypothesis that apraxia severity is strongly correlated with disease severity.Methods:Ninety participants in different stages of AD (mild, moderate, and s

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2

Roth, Heidi L., Thomas A. Eskin, Diane L. Kendall, and Kenneth M. Heilman. "Progressive Oculo-Orofacial-Speech Apraxia (POOSA)." Neurocase 12, no. 4 (2006): 221–27. http://dx.doi.org/10.1080/13554790600837347.

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3

Pita Lobo, Patrícia, Susana Pinto, Luz Rocha, Sofia Reimão, and Mamede de Carvalho. "Orofacial Apraxia in Motor Neuron Disease." Case Reports in Neurology 5, no. 1 (2013): 47–51. http://dx.doi.org/10.1159/000349895.

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4

Cera, Maysa, Karin Ortiz, Paulo Bertolucci, and Thais Minett. "P1-399: Apraxia of speech and orofacial apraxia in Alzheimer's disease." Alzheimer's & Dementia 7 (July 2011): S240. http://dx.doi.org/10.1016/j.jalz.2011.05.680.

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5

Gubiani, Marileda Barichello, Karina Carlesso Pagliarin, and Marcia Keske-Soares. "Instrumentos para avaliação de apraxia de fala infantil." CoDAS 27, no. 6 (2015): 610–15. http://dx.doi.org/10.1590/2317-1782/20152014152.

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RESUMO Objetivo: Revisar sistematicamente na literatura os principais instrumentos utilizados para avaliação da apraxia de fala infantil. Estratégia de pesquisa: Realizou-se busca nas bases Scopus, PubMed e Embase Critérios de seleção: Foram selecionados estudos empíricos que utilizaram instrumentos de avaliação da apraxia de fala infantil. Análise dos dados: A seleção dos artigos foi realizada por dois pesquisadores independentes. Resultados: Foram encontrados 695 resumos. Após a leitura dos resumos, foram selecionados 12 artigos completos. Foi possível identificar cinco instrumentos: Verbal

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6

�zsancak, Canan, Pascal Auzou, and Didier Hannequin. "Dysarthria and orofacial apraxia in corticobasal degeneration." Movement Disorders 15, no. 5 (2000): 905–10. http://dx.doi.org/10.1002/1531-8257(200009)15:5<905::aid-mds1022>3.0.co;2-d.

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7

McNeil, Malcolm R., Gary Weismer, Scott Adams, and Moira Mulligan. "Oral Structure Nonspeech Motor Control in Normal, Dysarthric, Aphasic and Apraxic Speakers." Journal of Speech, Language, and Hearing Research 33, no. 2 (1990): 255–68. http://dx.doi.org/10.1044/jshr.3302.255.

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This study investigated the isometric force and static position control of the upper lip, lower lip, tongue, jaw, and finger in four subject groups (normal control, apraxia of speech, conduction aphasia, and ataxic dysarthria) at two force and displacement levels. Results from both the force and position tasks suggested that the apraxic and dysarthric groups tended to produce significantly greater instability than the normal group, although the pattern of instability across articulators was not systematic within or across the force and position experiments for subjects within or between groups

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8

Bhardwaj, Parveen, Minoo Sharma, and Karan Ahluwalia. "Joubert Syndrome with Orofacial Digital Features." Journal of Neurosciences in Rural Practice 09, no. 01 (2018): 152–54. http://dx.doi.org/10.4103/jnrp.jnrp_338_17.

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ABSTRACTJoubert syndrome (JS) is an autosomal recessive inherited disorder characterized by hypotonia, cerebellar vermis hypoplasia, ocular abnormalities (e.g., pigmentary retinopathy, oculomotor apraxia, and nystagmus), renal cysts, and hepatic fibrosis. Respiratory abnormalities, as apnea and hyperpnea, may be present, as well as mental retardation. Since the clinical findings of JS are quite heterogeneous, determination of radiological findings is essential.

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9

Tomaiuolo, Francesco, Serena Campana, Loredana Voci, Stefano Lasaponara, Fabrizio Doricchi, and Michael Petrides. "The Precentral Insular Cortical Network for Speech Articulation." Cerebral Cortex 31, no. 8 (2021): 3723–31. http://dx.doi.org/10.1093/cercor/bhab043.

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Abstract Apraxia of speech is a motor disorder characterized by the impaired ability to coordinate the sequential articulatory movements necessary to produce speech. The critical cortical area(s) involved in speech apraxia remain controversial because many of the previously reported cases had additional aphasic impairments, preventing localization of the specific cortical circuit necessary for the somatomotor execution of speech. Four patients with “pure speech apraxia” (i.e., who had no aphasic and orofacial motor impairments) are reported here. The critical lesion in all four patients involv

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10

Ray, Jayanti. "Effects of orofacial myofunctional therapy on speech intelligibility in individuals with persistent articulatory impairments." International Journal of Orofacial Myology 29, no. 1 (2003): 5–14. http://dx.doi.org/10.52010/ijom.2003.29.1.1.

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This study examined the effects of orofacial myofunctional therapy (OMT) on speech intelligibility in adults with persistent articulation impairments. Six adults in the age range of 18-23 years were selected to receive orofacial myofunctional therapy for a period of six weeks. The results showed that five out of six clients made significant progress in oral postures and speech sound production across all three speech production tasks: single words, sentences, and spontaneous speech. Speech intelligibility increased significantly in all clients except the one diagnosed with developmental apraxi

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11

Chang, Edward F., Garret Kurteff, John P. Andrews, et al. "Pure Apraxia of Speech After Resection Based in the Posterior Middle Frontal Gyrus." Neurosurgery 87, no. 3 (2020): E383—E389. http://dx.doi.org/10.1093/neuros/nyaa002.

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Abstract BACKGROUND AND IMPORTANCE Apraxia of speech is a disorder of articulatory coordination and planning in speech sound production. Its diagnosis is based on deficits in articulation, prosody, and fluency. It is often described concurrent with aphasia or dysarthria, while pure apraxia of speech is a rare entity. CLINICAL PRESENTATION A right-handed man underwent focal surgical resection of a recurrent grade III astrocytoma in the left hemisphere dorsal premotor cortex located in the posterior middle frontal gyrus. After the procedure, he experienced significant long-term speech production

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12

Trebbastoni, Alessandro, Fabrizia D’Antonio, Carlo de Lena, Emanuela Onesti, Bev John, and Maurizio Inghilleri. "Primary Progressive Orofacial Apraxia: A Ten-Year Long Follow-Up Case Report." Journal of Alzheimer's Disease 54, no. 3 (2016): 1039–45. http://dx.doi.org/10.3233/jad-160525.

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13

Ozsancak, Canan, Pascal Auzou, Kathy Dujardin, Niall Quinn, and Alain Dest�e. "Orofacial apraxia in corticobasal degeneration, progressive supranuclear palsy, multiple system atrophy and Parkinson?s disease." Journal of Neurology 251, no. 11 (2004): 1317–23. http://dx.doi.org/10.1007/s00415-004-0530-0.

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14

Nan, Haitian, Ryusuke Takaki, Yuta Ichinose, et al. "Novel SLC20A2 mutation in primary familial brain calcification with disturbance of sustained phonation and orofacial apraxia." Journal of the Neurological Sciences 390 (July 2018): 1–3. http://dx.doi.org/10.1016/j.jns.2018.03.031.

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15

Carrigg, Bronwyn, Louise Parry, Elise Baker, Lawrence D. Shriberg, and Kirrie J. Ballard. "Cognitive, Linguistic, and Motor Abilities in a Multigenerational Family with Childhood Apraxia of Speech." Archives of Clinical Neuropsychology 31, no. 8 (2016): 1006–25. http://dx.doi.org/10.1093/arclin/acw077.

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Abstract Objective This study describes the phenotype in a large family with a strong, multigenerational history of severe speech sound disorder (SSD) persisting into adolescence and adulthood in approximately half the cases. Aims were to determine whether a core phenotype, broader than speech, separated persistent from resolved SSD cases; and to ascertain the uniqueness of the phenotype relative to published cases. Method Eleven members of the PM family (9–55 years) were assessed across cognitive, language, literacy, speech, phonological processing, numeracy, and motor domains. Between group

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16

Oliveira, Ecila Paula dos Mesquita de, Marina Liberalesso Neri, Lívia Lucena de Medeiros, Catarina Abraão Guimarães, and Marilisa Mantovani Guerreiro. "Avaliação do desempenho escolar e praxias em crianças com Epilepsia Rolândica." Pró-Fono Revista de Atualização Científica 22, no. 3 (2010): 209–14. http://dx.doi.org/10.1590/s0104-56872010000300009.

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TEMA: Epilepsia Rolândica é a forma mais freqüente de epilepsia da infância. Ela é classificada como idiopática, idade-dependente e de evolução benigna. A ausência de comprometimento neuropsicológico faz parte dos critérios de benignidade desta síndrome epiléptica.Entretanto, recentemente têm sido sugeridos vários déficits relacionados à atenção e linguagem. OBJETIVO: o objetivo desse trabalho foi avaliar o desempenho escolar e investigar dificuldades práxicas em pacientes com epilepsia rolândica e comparar a um grupo controle composto por crianças normais com idade, gênero e nível escolar equ

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17

Cera, Maysa Luchesi, Karin Zazo Ortiz, Paulo Henrique Ferreira Bertolucci, and Thaís Soares Cianciarullo Minett. "Speech and orofacial apraxias in Alzheimer's disease – CORRIGENDUM." International Psychogeriatrics 25, no. 10 (2013): 1686. http://dx.doi.org/10.1017/s1041610213001208.

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18

Machado, Yasmin Valente, Jadenn Rubia Lima Costa, Julianna Lacerda Facundo, and Myllena Gomes Silva. "ALTERAÇÕES DE LINGUAGEM ORAL NA APRAXIA DE FALA IDIOPÁTICA INFANTO-JUVENIL: UMA REVISÃO INTEGRATIVA." Centro de Pesquisas Avançadas em Qualidade de Vida, v12n3 (2020): 1–8. http://dx.doi.org/10.36692/v12n3-22r.

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A apraxia de fala é uma desorganização motora, prejudicando a programação e execução dos movimentos orofaciais fundamentais para a realização dos fonemas, e quando atinge as crianças, elas sentem mais dificuldades se comparadas a crianças que possuam distúrbios de fala e linguagem de outros gêneros. O objetivo do estudo foi verificar o cenário nacional e internacional através de publicações atuais sobre as principais alterações identificadas na linguagem oral de pacientes infantis e jovens apráxicos idiopáticos. Trata-se de uma revisão integrativa de literatura, por meio de buscas nas bases de

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19

Félix, Paloma Ludimila Cunha, Ivonaldo Leidson Barbosa Lima, Giorvan Ânderson dos Santos Alves, and Rafael Nóbrega Bandeira. "Achados fonoaudiológicos em caso de síndrome de Sjögren após acidentes vasculares cerebrais múltiplos." Distúrbios da Comunicação 32, no. 3 (2020): 510–16. http://dx.doi.org/10.23925/2176-2724.2020v32i3p510-516.

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Este trabalho objetivou descrever os achados fonoaudiológicos de uma paciente com Síndrome de Sjögren, vítima de múltiplos Acidentes Vasculares Cerebrais. Para isso, foi realizado um relato de um caso diagnosticado com Síndrome de Sjögren e AVC Múltiplos. A avaliação fonoaudiológica foi realizada por meio da anamnese neurológica, aplicação do Protocolo de MBGR, o Protocolo para Avaliação da Apraxia da Fala, Protocolo de Avaliação da Disartria, Bateria de Rastreio Cognitivo e o Protocolo de Atividades de Vida Diária. Observou-se, na avaliação das estruturas orofaciais, uma língua com altura e l

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20

Martins, Fernanda Cristina Reis Merli, Fernanda Prada Machado, Caroline Santos Rodrigues da Silva, and Ruth Ramalho Ruivo Palladino. "Avaliação da apraxia de fala na infância no transtorno do espectro autista: relato de três casos clínicos." ABCS Health Sciences 46 (March 8, 2021): e021401. http://dx.doi.org/10.7322/abcshs.2019165.1434.

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Introdução: Dentre as dificuldades de comunicação encontradas em casos de Transtornos do Espectro do Autismo (TEA), recentemente a literatura tem apontado uma relação de comorbidade com a apraxia de fala na infância (AFI). O objetivo do presente estudo foi relatar a avaliação de AFI em 3 crianças com diagnóstico de TEA. Relato: Os sujeitos foram três crianças com idades entre 4 e 6 anos, com diagnóstico médico de TEA. Os sujeitos foram submetidos à avaliação de linguagem, utilizando o teste avaliação de desenvolvimento da linguagem (ADL) e a prova de vocabulário do teste ABFW, avaliação das pr

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21

Guilleminault, Christian, Yu-Shu Huang, and Stacey Quo. "Apraxia in children and adults with obstructive sleep apnea syndrome." Sleep 42, no. 12 (2019). http://dx.doi.org/10.1093/sleep/zsz168.

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Abstract Study Objectives Early in life impairment of orofacial growth leads to sleep-disordered breathing (SDB). Normal lingual gnosis and praxis are part of this early development related to the normal sensorimotor development of the tongue and surrounding oral musculature. The aim of this retrospective study was to explore if lingual praxia is impaired in both SDB children and adults and if there is an association to craniofacial morphology. Methods The ability to perform simple tongue maneuvers was investigated in 100 prepubertal SDB children and 150 SDB adults (shown with polysomnography)

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22

Torres, Geciane Xavier, Emerson de Santana Santos, Carla Patrícia Hernandez Alves Ribeiro César, Roxane de Alencar Irineu, Isabel Ribeiro Rocha Dias, and Alice Fontes Ramos. "Clinical orofacial and myofunctional manifestations in an adolescent with Noonan Syndrome: a case report." Revista CEFAC 22, no. 4 (2020). http://dx.doi.org/10.1590/1982-0216/202022416519.

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ABSTRACT Noonan syndrome is an autosomal dominant genetic disease with different manifestations, including Speech, Language and Hearing Sciences ones. The authors describe the orofacial and myofunctional manifestations of an adolescent diagnosed with Noonan syndrome, by consulting the Speech, Language and Hearing Sciences record of a 17-year-old male patient, who underwent screening and speech therapy evaluation with a confirmed genetic diagnosis of Noonan syndrome. The results were qualitatively analyzed. The patient had a long facial type, with a disproportion between the lower and middle th

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