Results 101 to 110 of about 2,544 (214)
Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review [PDF]
, 2014 Objectives: In the present study, it is described the phenotypical analysis and the mutational screening, for genes PAX9 and MSX1, of six families affected by severe forms of tooth agenesis associated with other dental anomalies and systemic entities ...
Arte, Sirpa +5 more
core +1 more source
Dental anomalies in an orthodontic patient population with maxillary lateral incisor agenesis
Dental Press Journal of OrthodonticsIntroduction: The purpose of this study was to evaluate the prevalence of dental anomalies in a subpopulation of orthodontic patients with agenesis of maxillary lateral incisors (MLI).
Mehmet Citak +5 more
doaj +1 more source
Case Reports in Dentistry, 2018 Taurodontism is considered a dental anomaly responsible for a morphoanatomical change in the shape of the tooth in which the roots are reduced in size but the body of the tooth is enlarged and bulky.
Polianne Alves Mendes +4 more
doaj +1 more source
Journal of Dental Sciences, 2015 Background/purpose: There is remarkably little information in the literature comparing the prevalence of dental anomalies associated with mandibular second premolar (MP2) agenesis with control groups.
Kenan Cantekin, Mevlut Celikoglu
doaj +1 more source
Correction to: Taurodontism [PDF]
Oral Radiology, 2019 In the original publication of the article, few errors were identified. The corrections are given below:
openaire +1 more source
Amelogenesis Imperfecta with Taurodontism, Microdontia, and Minor Thalassemia: A Case Report [PDF]
Journal of Dental Materials and Techniques, 2013 Amelogenesis imperfecta is a group of genetic disorders that affects both the morphology and quality of tooth structure. Although the disease entity is primarily associated with abnormalities of dental and oral structures, it has been reported to be ...
Fatemeh Mazhari +1 more
doaj
Amelogénesis imperfecta tipo IE. a propósito de una familia afectada [PDF]
, 2016 En este artículo se revisa el concepto de Amelogénesis imperfecta a propósito de una familia afectada de Amelogénesis imperfecta tipo lE, según la clasificación de WITKOP.
Chimenos Küstner, Eduardo +3 more
core
A critical evaluation of the Down syndrome diagnosis for LB1, type specimen of Homo floresiensis [PDF]
, 2016 The Liang Bua hominins from Flores, Indonesia, have been the subject of intense scrutiny and debate since their initial description and classification in 2004.
Baab, Karen L +6 more
core +4 more sources
Tricho-Dento-Osseous Syndrome: Diagnosis and Dental Management
International Journal of Dentistry, 2012 Tricho-dento-osseous (TDO) syndrome is a rare, autosomal dominant disorder principally characterised by curly hair at infancy, severe enamel hypomineralization and hypoplasia and taurodontism of teeth, sclerotic bone, and other defects.
Ola B. Al-Batayneh
doaj +1 more source
Oligodontia with taurodontism in monozygous twins
North American Journal of Medical Sciences, 2012 Dear Editor, A wide spectrum of developmental pathologies affects the teeth, which includes variation in shape, size, eruption pattern, and number. Tooth agenesis is one such condition that leads to hypodontia and oligodontia. Prevalence of hypodontia was found to be 1.6% to 9.6% in the permanent dentition.
Kandagal, V Suresh +5 more
openaire +3 more sources