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Impact of rare diseases in oral health
BACKGROUND: Rare diseases (RD) are those that present a lower prevalence than 5 cases per 10.000 population. The main objective of this review was to study the effect on oral health in rare diseases, while the secondary objective of the study is theme upgrade. MATERIAL AND METHODS: Comparative obser...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medicina Oral S.L.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005096/ https://www.ncbi.nlm.nih.gov/pubmed/27475682 http://dx.doi.org/10.4317/medoral.20972 |
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author | Molina-García, Ana Castellanos-Cosano, Lizett Machuca-Portillo, Guillermo Posada-de la Paz, Manuel |
author_facet | Molina-García, Ana Castellanos-Cosano, Lizett Machuca-Portillo, Guillermo Posada-de la Paz, Manuel |
author_sort | Molina-García, Ana |
collection | PubMed |
description | BACKGROUND: Rare diseases (RD) are those that present a lower prevalence than 5 cases per 10.000 population. The main objective of this review was to study the effect on oral health in rare diseases, while the secondary objective of the study is theme upgrade. MATERIAL AND METHODS: Comparative observational case-control studies were analysed and a systematic review was conducted in PubMed. Each rare disease listed on the statistical data record of the Health Portal of the Ministry of Equality, Health and Social Policies Board of Andalusia was associated with “oral health”. The variables studied included dental, oral mucosa and occlusion alterations, oral pathologies (caries, periodontal disease) and other alterations (mouth breathing, parafunctional habits, etc). A bias analysis of the variable caries was conducted. RESULTS: Six RD were selected through our inclusion and exclusion criteria (hypogammaglobulinemia, Rett syndrome, Marfan syndrome, Prader-Willi syndrome, cystic fibrosis and Cri du chat syndrome) in a total of 8 publications, of which four trials were classified as high risk of bias and one of them as medium risk. There were not trials with low risk of bias. CONCLUSIONS: The main statistically significant differences found by Syndrome compared to a control group were in Hypogammaglobulinemia with a greater tendency to enamel hypoplasia and dry mouth. The Rett syndrome had, as well, a greater tendency to an anterior open bite, ogival palate, bruxism, mouth breathing and tongue thrusting. Prader-Willi syndrome had a tendency of dental erosion, and Cri du chat syndrome showed a higher association to Tannerella forsythia. Key words:Rare diseases, oral health. |
format | Online Article Text |
id | pubmed-5005096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medicina Oral S.L. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50050962016-09-01 Impact of rare diseases in oral health Molina-García, Ana Castellanos-Cosano, Lizett Machuca-Portillo, Guillermo Posada-de la Paz, Manuel Med Oral Patol Oral Cir Bucal Review BACKGROUND: Rare diseases (RD) are those that present a lower prevalence than 5 cases per 10.000 population. The main objective of this review was to study the effect on oral health in rare diseases, while the secondary objective of the study is theme upgrade. MATERIAL AND METHODS: Comparative observational case-control studies were analysed and a systematic review was conducted in PubMed. Each rare disease listed on the statistical data record of the Health Portal of the Ministry of Equality, Health and Social Policies Board of Andalusia was associated with “oral health”. The variables studied included dental, oral mucosa and occlusion alterations, oral pathologies (caries, periodontal disease) and other alterations (mouth breathing, parafunctional habits, etc). A bias analysis of the variable caries was conducted. RESULTS: Six RD were selected through our inclusion and exclusion criteria (hypogammaglobulinemia, Rett syndrome, Marfan syndrome, Prader-Willi syndrome, cystic fibrosis and Cri du chat syndrome) in a total of 8 publications, of which four trials were classified as high risk of bias and one of them as medium risk. There were not trials with low risk of bias. CONCLUSIONS: The main statistically significant differences found by Syndrome compared to a control group were in Hypogammaglobulinemia with a greater tendency to enamel hypoplasia and dry mouth. The Rett syndrome had, as well, a greater tendency to an anterior open bite, ogival palate, bruxism, mouth breathing and tongue thrusting. Prader-Willi syndrome had a tendency of dental erosion, and Cri du chat syndrome showed a higher association to Tannerella forsythia. Key words:Rare diseases, oral health. Medicina Oral S.L. 2016-09 2016-07-31 /pmc/articles/PMC5005096/ /pubmed/27475682 http://dx.doi.org/10.4317/medoral.20972 Text en Copyright: © 2016 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Molina-García, Ana Castellanos-Cosano, Lizett Machuca-Portillo, Guillermo Posada-de la Paz, Manuel Impact of rare diseases in oral health |
title | Impact of rare diseases in oral health |
title_full | Impact of rare diseases in oral health |
title_fullStr | Impact of rare diseases in oral health |
title_full_unstemmed | Impact of rare diseases in oral health |
title_short | Impact of rare diseases in oral health |
title_sort | impact of rare diseases in oral health |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005096/ https://www.ncbi.nlm.nih.gov/pubmed/27475682 http://dx.doi.org/10.4317/medoral.20972 |
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