Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review
Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and variable tissue fragility. However, there are limited published data on the dental manifestations of EDS. This review systematically assessed the spec...
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Society for Publication of Acta Dermato-Venereologica
2020-03-01
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https://www.medicaljournals.se/acta/content/html/10.2340/00015555-3428
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doaj-d1f467c926f649a68b345d71baae6e342020-11-25T02:04:49ZengSociety for Publication of Acta Dermato-VenereologicaActa Dermato-Venereologica0001-55551651-20572020-03-011007adv0009210.2340/00015555-34285688Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic ReviewInes Kapferer-Seebacher0Dagmar SchnablJohannes ZschockeF. Michael Pope Department of Operative and Restorative Dentistry, Medical University Innsbruck, Innsbruck, Austria. Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and variable tissue fragility. However, there are limited published data on the dental manifestations of EDS. This review systematically assessed the spectrum of published dental anomalies in various types of EDS. Twenty-four individual case reports/series and 3 longer case-control studies, reporting on a total of 84 individuals with a clinical diagnosis of EDS, were included in the data analysis. The main dental features listed in classical EDS were pulp calcification and localized root hypoplasia. Common dental abnormalities observed in vascular EDS were pulp shape modifications (52.2%), exceeding root length (34.8%), and molar root fusion (47.8%). Dentinogenesis imperfecta is a consistent finding in osteogenesis imperfecta/EDS overlap syndrome. Data on dental manifestations in other types of EDS are both rare and generally inconclusive. https://www.medicaljournals.se/acta/content/html/10.2340/00015555-3428 ehlers-danlos syndromes hypermobility oral manifestation dental anomaly |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ines Kapferer-Seebacher Dagmar Schnabl Johannes Zschocke F. Michael Pope |
spellingShingle |
Ines Kapferer-Seebacher Dagmar Schnabl Johannes Zschocke F. Michael Pope Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review Acta Dermato-Venereologica ehlers-danlos syndromes hypermobility oral manifestation dental anomaly |
author_facet |
Ines Kapferer-Seebacher Dagmar Schnabl Johannes Zschocke F. Michael Pope |
author_sort |
Ines Kapferer-Seebacher |
title |
Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review |
title_short |
Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review |
title_full |
Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review |
title_fullStr |
Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review |
title_full_unstemmed |
Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review |
title_sort |
dental manifestations of ehlers-danlos syndromes: a systematic review |
publisher |
Society for Publication of Acta Dermato-Venereologica |
series |
Acta Dermato-Venereologica |
issn |
0001-5555 1651-2057 |
publishDate |
2020-03-01 |
description |
Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and variable tissue fragility. However, there are limited published data on the dental manifestations of EDS. This review systematically assessed the spectrum of published dental anomalies in various types of EDS. Twenty-four individual case reports/series and 3 longer case-control studies, reporting on a total of 84 individuals with a clinical diagnosis of EDS, were included in the data analysis. The main dental features listed in classical EDS were pulp calcification and localized root hypoplasia. Common dental abnormalities observed in vascular EDS were pulp shape modifications (52.2%), exceeding root length (34.8%), and molar root fusion (47.8%). Dentinogenesis imperfecta is a consistent finding in osteogenesis imperfecta/EDS overlap syndrome. Data on dental manifestations in other types of EDS are both rare and generally inconclusive. |
topic |
ehlers-danlos syndromes hypermobility oral manifestation dental anomaly |
url |
https://www.medicaljournals.se/acta/content/html/10.2340/00015555-3428
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work_keys_str_mv |
AT ineskapfererseebacher dentalmanifestationsofehlersdanlossyndromesasystematicreview AT dagmarschnabl dentalmanifestationsofehlersdanlossyndromesasystematicreview AT johanneszschocke dentalmanifestationsofehlersdanlossyndromesasystematicreview AT fmichaelpope dentalmanifestationsofehlersdanlossyndromesasystematicreview |
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1724940948370096128 |