Review Article
Be Pointed Study of the Relation of Molar and Incisors Hypomineralization Incidence in Patients of Ehlers-Danlos
Ana Paula Penitente1, Idiberto Jose Zotarelli Filho1,2*, Taylane Soffener Berlanga de Araújo1,2, Maira Regina1, Andreia Borges Scriboni1 and Elias Naim Kassis1,2
1Department of Odontology, University Center North Paulista, Brazil
2Department of Regenerative Medicine and Tissue Engineering, Universidade Estadual Paulista, Brazil
- Corresponding Author:
- Idiberto José Zotarelli Filho
Department of Odontology
University Center North Paulista
Street Ipiranga, 3460, São José do Rio Preto SP
15020-040, Brazil
Tel: +55 17 98166-6537
E-mail: m.zotarelli@gmail.com
Received date: April 23, 2015; Accepted date: June 05, 2015; Published date: June 09, 2015
Citation: Penitente AP, Filho IJZ, Araújo TSBD, Regina M, Scriboni AB, et al. (2015) Be Pointed Study of the Relation of Molar and Incisors Hypomineralization Incidence in Patients of Ehlers-Danlos. J Interdiscipl Med Dent Sci 3:179. doi: 10.4172/2376-032X.1000179
Copyright: © 2015 Penitente AP, et al. 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 author and source are credited.
Abstract
The hypomineralization is a pathology that has great clinical relevance, where the affected dental enamel presents areas of discoloration, with higher fracture risk, high risk caries and high sensitivity. The aim of work was to perform a survey of possible carriers of Ehlers-Danlos syndrome (EDS), through the Beighton test, which is attributed to a heterogeneous group of genetic amendments of the structure and collagen synthesis and connective tissue and be able to associate the relationship the incidence of MIH in this group. Because it is known that collagen is of paramount importance to dental development, and if occurs the interference by addition of destructive agents in their midst this will inhibit tooth morphogenesis. As the diagnostic of this syndrome in childhood is very difficult because children are more flexible, associate the detection of the presence of MIH may alert the investigation of Ehrles-Danlos syndrome, demonstrating the severity of structural anomalies, in this manner the early treatment can improve the quality of life of this population group.