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dc.rights.license |
CC BY NC ND |
eng |
dc.contributor.author |
Klimova, Blanka |
cze |
dc.contributor.author |
Valis, Martin |
cze |
dc.contributor.author |
Hort, Jakub |
cze |
dc.contributor.author |
Kuča, Kamil |
cze |
dc.date.accessioned |
2020-06-07T21:16:05Z |
|
dc.date.available |
2020-06-07T21:16:05Z |
|
dc.date.issued |
2019 |
eng |
dc.identifier.issn |
1214-021X |
eng |
dc.identifier.uri |
http://hdl.handle.net/20.500.12603/355 |
|
dc.description.abstract |
The purpose of this review is to discuss rare neurological disorders with respect to communication difficulties typical of children. Firstly, communication disorders with special focus on rare communication neurological disorders are discussed. Secondly, on the basis of literature review, the authors explore clinical studies on the most typical rare children's communication neurological disorders. Thirdly, on the basis of the findings from the clinical studies, they set a few recommendations for their medical therapies and management. The methodology was based on the literature review of research studies exploring the research issue. The findings show that the intervention strategies appear to have positive effects on the improvement of speech and language production among children suffering from Landau-Kleffner syndrome and childhood apraxia of speech. Nevertheless, randomized control trials are needed in order to accelerate and facilitate an early and relevant diagnosis and treatment management. In addition, a multidisciplinary approach seems to be the most appropriate for the accurate diagnosis and comprehensive treatment. |
eng |
dc.format |
p. 29-33 |
eng |
dc.language.iso |
eng |
eng |
dc.publisher |
Jihočeská univerzita |
eng |
dc.relation.ispartof |
Journal of applied biomedicine, volume 17, issue: 1 |
eng |
dc.subject |
Childhood apraxia of speech |
eng |
dc.subject |
Communication |
eng |
dc.subject |
Landau-Kleffner syndrome |
eng |
dc.subject |
Language |
eng |
dc.subject |
Neurological disorders |
eng |
dc.subject |
Treatment |
eng |
dc.subject |
Dětská apraxie řeči |
cze |
dc.subject |
Sdělení |
cze |
dc.subject |
Landau-Kleffnerův syndrom |
cze |
dc.subject |
Jazyk |
cze |
dc.subject |
Neurologické poruchy |
cze |
dc.subject |
Léčba |
cze |
dc.title |
Selected rare paediatric communication neurological disorders |
eng |
dc.title.alternative |
Vybrané vzácné pediatrické komunikační neurologické poruchy |
cze |
dc.type |
article |
eng |
dc.identifier.obd |
43875718 |
eng |
dc.identifier.wos |
000493806600004 |
eng |
dc.identifier.doi |
10.32725/jab.2018.002 |
eng |
dc.description.abstract-translated |
The purpose of this review is to discuss rare neurological disorders with respect to communication difficulties typical of children. Firstly, communication disorders with special focus on rare communication neurological disorders are discussed. Secondly, on the basis of literature review, the authors explore clinical studies on the most typical rare children's communication neurological disorders. Thirdly, on the basis of the findings from the clinical studies, they set a few recommendations for their medical therapies and management. The methodology was based on the literature review of research studies exploring the research issue. The findings show that the intervention strategies appear to have positive effects on the improvement of speech and language production among children suffering from Landau-Kleffner syndrome and childhood apraxia of speech. Nevertheless, randomized control trials are needed in order to accelerate and facilitate an early and relevant diagnosis and treatment management. In addition, a multidisciplinary approach seems to be the most appropriate for the accurate diagnosis and comprehensive treatment. |
cze |
dc.publicationstatus |
postprint |
eng |
dc.peerreviewed |
yes |
eng |
dc.source.url |
https://jab.zsf.jcu.cz/pdfs/jab/2019/01/04.pdf |
cze |
dc.relation.publisherversion |
https://jab.zsf.jcu.cz/pdfs/jab/2019/01/04.pdf |
eng |
dc.rights.access |
Open Access |
eng |
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