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Displasia ectodérmica: impactos na cavidade oral
| Name: | Description: | Size: | Format: | |
|---|---|---|---|---|
| PPG_31337 | 260.99 KB | Adobe PDF |
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Abstract(s)
Introdução: A displasia ectodérmica é uma doença genética e hereditária caracterizada por uma anomalia das estruturas ectodérmicas. Associa-se a uma tríade típica: hipoidrose, oligodontia e hipotricose.
Objetivo: O presente trabalho tem como objetivos explorar a temática: displasia ectodérmica hipoidrótica , relacioná-la com os impactos sentidos na cavidade oral e discutir a importância da multidisciplinariedade neste contexto.
Metodologia: Revisão narrativa, nos motores de busca: Sciencedirect, B-on, Elsevier e Pubmed, no período (2005-2018), com as palavres-chave «Displasia ectodérmica», «Hipodontia/anodontia», «Genética», «Reabilitação oral», «Síndrome de Touraine Siemens».
Conclusão: A displasia ectodérmica permanece uma patologia rara caracterizada por anormalidades na morfogénese de tecidos e órgãos de origem ectodérmica. As anomalias dentárias associadas têm consequências no crescimento crânio-cervico-facial. A displasia ectodérmica requer prevenção e tratamento em Medicina Dentária, sempre numa abordagem multidisciplinar.
Introduction: Ectodermal dysplasia is a genetic and hereditary disease characterized by an anomaly of ectodermal structures. It is associated with a typical triad: hypohidrosis, oligodontia, and hypotrichosis. Objective: The present work aims to explore the theme: hypohidrotic ectodermal dysplasia, to relate it to the impacts felt in the oral cavity and to discuss the importance of multidisciplinarity in this context. Methodology: Narrative review in the search engines: Sciencedirect, B-on, Elsevier and Pubmed, in the period (2005-2018), with the key words «Ectodermal dysplasia», «Hipodontia / anodontia», «Genetics», «Oral rehabilitation» , "Touraine Siemens Syndrome". Conclusion : DE remains a rare condition characterized by abnormalities in morphogenesis of tissues and organs of ectodermal origin induced by a genetic disorder. Dental anomalies have consequences on facial growth and maxillary growth. DE requires prevention and treatment in dental medicine include motivation for oral hygiene, conservative care, orthodontics and prosthetic rehabilitation.
Introduction: Ectodermal dysplasia is a genetic and hereditary disease characterized by an anomaly of ectodermal structures. It is associated with a typical triad: hypohidrosis, oligodontia, and hypotrichosis. Objective: The present work aims to explore the theme: hypohidrotic ectodermal dysplasia, to relate it to the impacts felt in the oral cavity and to discuss the importance of multidisciplinarity in this context. Methodology: Narrative review in the search engines: Sciencedirect, B-on, Elsevier and Pubmed, in the period (2005-2018), with the key words «Ectodermal dysplasia», «Hipodontia / anodontia», «Genetics», «Oral rehabilitation» , "Touraine Siemens Syndrome". Conclusion : DE remains a rare condition characterized by abnormalities in morphogenesis of tissues and organs of ectodermal origin induced by a genetic disorder. Dental anomalies have consequences on facial growth and maxillary growth. DE requires prevention and treatment in dental medicine include motivation for oral hygiene, conservative care, orthodontics and prosthetic rehabilitation.
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Keywords
Displasia ectodérmica Hipodontia/anodontia Genética Reabilitação oral Síndrome de Touraine Siemens Ectodermal dysplasia Hipodontia / anodontia Genetics Oral rehabilitation Touraine Siemens syndrome