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Brain areas impaired in oral and verbal apraxic patients

Background: As both oral and verbal apraxia are related to vocal orofacial musculature, this study aimed at identifying brain regions impaired in cases with oral and verbal apraxia. Methods: In this non-experimental study, 46 left brain damaged subjects (17 females) aged 23–84 years, were examined b...

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Autores principales: Yadegari, Fariba, Azimian, Mojtaba, Rahgozar, Mahdi, Shekarchi, Babak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Neurological Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187334/
https://www.ncbi.nlm.nih.gov/pubmed/25295150
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author Yadegari, Fariba
Azimian, Mojtaba
Rahgozar, Mahdi
Shekarchi, Babak
author_facet Yadegari, Fariba
Azimian, Mojtaba
Rahgozar, Mahdi
Shekarchi, Babak
author_sort Yadegari, Fariba
collection PubMed
description Background: As both oral and verbal apraxia are related to vocal orofacial musculature, this study aimed at identifying brain regions impaired in cases with oral and verbal apraxia. Methods: In this non-experimental study, 46 left brain damaged subjects (17 females) aged 23–84 years, were examined by oral and verbal apraxia tasks. Impaired and spared Broca’s area, insula, and middle frontal gyrus in the left hemisphere were checked from magnetic resonance imaging and computed tomography scans utilizing Talairach Atlas. Data were analyzed using chi-square test. Results: Insula was significantly impaired in both forms of oral and verbal apraxia and different severities and prominent forms of both apraxias (P < 0.05). Broca’s area was slightly less involved than insula in two forms of apraxia. Conclusion: As the damage of insula was more prominent in both forms of apraxias, it seems that oral and verbal apraxia may have commonalities regarding their underlying brain lesions.
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spelling pubmed-41873342014-10-07 Brain areas impaired in oral and verbal apraxic patients Yadegari, Fariba Azimian, Mojtaba Rahgozar, Mahdi Shekarchi, Babak Iran J Neurol Original Article Background: As both oral and verbal apraxia are related to vocal orofacial musculature, this study aimed at identifying brain regions impaired in cases with oral and verbal apraxia. Methods: In this non-experimental study, 46 left brain damaged subjects (17 females) aged 23–84 years, were examined by oral and verbal apraxia tasks. Impaired and spared Broca’s area, insula, and middle frontal gyrus in the left hemisphere were checked from magnetic resonance imaging and computed tomography scans utilizing Talairach Atlas. Data were analyzed using chi-square test. Results: Insula was significantly impaired in both forms of oral and verbal apraxia and different severities and prominent forms of both apraxias (P < 0.05). Broca’s area was slightly less involved than insula in two forms of apraxia. Conclusion: As the damage of insula was more prominent in both forms of apraxias, it seems that oral and verbal apraxia may have commonalities regarding their underlying brain lesions. Iranian Neurological Association 2014-04-03 /pmc/articles/PMC4187334/ /pubmed/25295150 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yadegari, Fariba
Azimian, Mojtaba
Rahgozar, Mahdi
Shekarchi, Babak
Brain areas impaired in oral and verbal apraxic patients
title Brain areas impaired in oral and verbal apraxic patients
title_full Brain areas impaired in oral and verbal apraxic patients
title_fullStr Brain areas impaired in oral and verbal apraxic patients
title_full_unstemmed Brain areas impaired in oral and verbal apraxic patients
title_short Brain areas impaired in oral and verbal apraxic patients
title_sort brain areas impaired in oral and verbal apraxic patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187334/
https://www.ncbi.nlm.nih.gov/pubmed/25295150
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