Communication in Huntington's Disease.
DOI:
https://doi.org/10.24054/rcsf.v7i2.1299Keywords:
Huntington's , communication , language in Huntington's , speech therapyAbstract
INTRODUCTION: The objective of this review is to learn about Huntington's disease, how it affects a person's performance in all spheres of life and the communicative process. METHODS: This article was prepared through a systematic review of scientific articles published in different databases such as: Science direct, Taylor & francis, Scielo, Pubmed, Revista de neurología, Google scholar, Dialnet and Revista chilena de neuropsicología. RESULTS: 60 articles were preselected, of which 35 were selected for the study. ANALYSIS AND DISCUSSION: The communicative profile in Huntington's disease is characterized by: a progressive loss of basic motor processes, mainly language and swallowing. CONCLUSIONS: Huntington's disease is a neurodegenerative disease that presents consequences at the physical, emotional, cognitive, communicative and social levels, which leads to people having a decrease in their quality of life and life expectancy.
Downloads
References
Kobal J, Cankar K, Pretnar J, Zaletel M, Kobal L, Teran N, et al. Functional impairment of precerebral arteries in Huntington disease. J Neurol Sci [Internet]. 2017;372:363–8. Available from: http://dx.doi.org/10.1016/j.jns.2016.10.033
Julayanont P, McFarland NR, Heilman KM. Mild cognitive impairment and dementia in motor manifest Huntington’s disease: Classification and prevalence. J Neurol Sci [Internet]. 2020;408(August 2019):116523. Available from: https://doi.org/10.1016/j.jns.2019.116523
Bartlett DM, Govus A, Rankin T, Lampit A, Feindel K, Poudel G, et al. The effects of multidisciplinary rehabilitation on neuroimaging, biological, cognitive and motor outcomes in individuals with premanifest Huntington’s disease. J Neurol Sci [Internet]. 2020;416(June):117022. Available from: https://doi.org/10.1016/j.jns.2020.117022
Montes, C., Llanos, A., y Soto, J. (2018). Los empleos de las personas con discapacidad. Convención Internacional de Salud. Cuba Salud, 3(21), 33-47.
Glikmann-Johnston Y, Carmichael AM, Mercieca EC, Stout JC. ‘Real-life’ hippocampal-dependent spatial memory impairments in Huntington’s disease. Cortex [Internet]. 2019;119:46–60. Available from: https://doi.org/10.1016/j.cortex.2019.04.006
Chan JCS, Stout JC, Vogel AP. Speech in prodromal and symptomatic Huntington’s disease as a model of measuring onset and progression in dominantly inherited neurodegenerative diseases. Neurosci Biobehav Rev [Internet]. 2019;107(April):450–60. Available from: https://doi.org/10.1016/j.neubiorev.2019.08.009
Ho AK, Horton MC, Landwehrmeyer GB, Burgunder JM, Tennant A, Downie L, et al. Meaningful and Measurable Health Domains in Huntington’s Disease: Large-Scale Validation of the Huntington’s Disease Health-Related Quality of Life Questionnaire Across Severity Stages. Value Heal. 2019;22(6):712–20.
Wilton DK, Stevens B. The contribution of glial cells to Huntington’s disease pathogenesis. Neurobiol Dis [Internet]. 2020;143(June):104963. Available from: https://doi.org/10.1016/j.nbd.2020.104963
Mestre TA. Recent advances in the therapeutic development for Huntington disease. Park Relat Disord [Internet]. 2019;59(August 2018):125–30. Available from: https://doi.org/10.1016/j.parkreldis.2018.12.003
Souza PVS de, Pedroso JL, Pinto WBV de R, Barsottini OGP. Huntington’s disease as an unexpected cause of deafness with dystonia and chorea. Park Relat Disord. 2020;76(June):10–2.
Brito D V., Della Coletta M V., Takano SA, Ferreira GBM, Fantin C. Genetic analysis of Huntington’s disease in a population from the Brazilian Amazon. Park Relat Disord [Internet]. 2020;78(July):94–5. Available from: https://doi.org/10.1016/j.parkreldis.2020.07.013
Mamédio C, Roberto M, Nobre C. the Pico Strategy for the Research Question. Rev latino-am Enferm. 2007;15(3):1–4.
Urrútia G, Bonfill X. Declaración PRISMA: una propuesta para mejorar la publicación de revisiones sistemáticas y metaanálisis. Vol. 135, Medicina Clínica. 2010. p. 507–11.
Ramírez SA, Colina S. Papel del fonoaudiólogo en el área de salud mental : una experiencia profesional en el hospital militar central. Rev Med. 2009;17(49):26–33.
Monrad P, Renaud DL. Typical clinical findings should prompt investigation for juvenile Huntington disease. Pediatr Neurol [Internet]. 2013;48(4):333–4. Available from: http://dx.doi.org/10.1016/j.pediatrneurol.2012.12.023
Muroni A, Murru MR, Sechi M, Ercoli T, Marrosu F, Bentivoglio AR, et al. Prevalence of Huntington’s disease in Southern Sardinia, Italy. Park Relat Disord [Internet]. 2020;80(April):54–7. Available from: https://doi.org/10.1016/j.parkreldis.2020.09.011
Camargo-Mendoza M, Castillo-Triana N, Fandiño-Cardona JM, Mateus-Moreno A, Moreno-Martínez M. Speech, language and swallowing in Huntington’ disease. Rev Fac Med. 2017;65(2):343–8.
Llanos Redondo, A., Rangel Navia, H. J., Aguilar Cañas, S. J., Tamara Moncada, V. A., & Crespo Pérez, N. C. (2020). Evaluación de anquiloglosia y lactancia materna en lactantes de 0 a 24 meses. Revista Salud Bosque, 10(2). https://doi.org/10.18270/rsb.v10i2.3015.
Arias G. Mortalidad debida a enfermedades raras en Europa: enfermedad de Huntington, ataxias hereditarias y enfermedades de la motoneurona. 2018;1–145.
Schiefer J. Compensation in the course of Huntington’s disease -More than just a hypothesis? EBioMedicine [Internet]. 2015;2(10):1286–7. Available from: http://dx.doi.org/10.1016/j.ebiom.2015.09.024
Rodríguez C. Caracterización de la Impulsividad Medida con la Escala de Impulsividad de Barrat (BIS-11) en una Muestra de Pacientes Colombianos con Enfermedad de Huntington. Univ Nac Colomb. 2016;
Tolosa-López S, Crespo-Pérez N , Llanos-Redondo A, Aguilar-Cañas S, Rangel-Navia H, Portilla-Portilla E, Rivera Porras D. Estudio comparativo de la Frecuencia Fundamental, Jitter y Shimmer en escolares normo oyentes e hipoacúsicos. Ciencia e Innovación en Salud. 2021. E142: 325-340 DOI http://dx.doi.org/10.17081/innosa.143
Gatto E, Parisi V, Persi G, Fernandez Rey E, Cesarini M, Luis Etcheverry J, et al. Optical coherence tomography (OCT) study in Argentinean Huntington’s disease patients. Int J Neurosci [Internet]. 2018;128(12):1157–62. Available from: https://doi.org/10.1080/00207454.2018.1489807
Espinoza-Suárez NR, Palacios-García J, Morante-Osores M del R. Cuidados paliativos en la enfermedad de Huntington: perspectivas desde la atención primaria de salud TT -Palliative care in Huntingtonïs disease: perspective from primary health care. Rev Neuropsiquiatr [Internet].
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2021 Zayda Rocío Peñaloza Montaño, Carlos Fabián Zambrano Muchavisoy
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
