Results 51 to 60 of about 7,575 (221)
Underdiagnosis of enamel defects in Family Health Centres of Talca city, Chile
Enamel defects (i.e. hypoplasia, diffuse and demarcated opacities), in particular Molar Incisor Hypomineralization (MIH), are alterations of dental enamel with underlying implications in affected children.
Carla Orellana-Herrera +3 more
doaj +1 more source
Cell Therapy for Periodontal, Soft‐Tissue, and Craniofacial Regeneration
The clinical translation of mesenchymal stem/stromal cells (MSCs) represents a major advancement in dentistry, especially for periodontal, soft‐tissue, and craniofacial regeneration. However, several challenges remain to be addressed, including the absence of standardised protocols, limited scalability, regulatory hurdles, a lack of well‐controlled ...
Kamal Mustafa +5 more
wiley +1 more source
ABSTRACT This systematic review aimed to collect and appraise the clinical outcomes of all orthopaedic, orthodontic and surgical interventions in ACH patients. Following PROSPERO protocol, multiple database sources were searched to December 2024 with no language restrictions for (i) genetically confirmed ACH; (ii) any orthodontic/orthopaedic ...
Marco Farronato +5 more
wiley +1 more source
Periodontal Architecture in Ectodermal Dysplasia: An Observational Clinical and Histological Study
ABSTRACT Objective To investigate gingival and periodontal characteristics in Ectodermal dysplasia (ED), focusing on soft‐tissue phenotype, anatomical variations, and periodontal architecture. Materials and Methods Observational clinical study of 11 individuals (16–30 years) with confirmed clinical or genetic ED diagnosis.
Marco Montevecchi +5 more
wiley +1 more source
Background: It is axiomatic that Pediatric dental anomalies and enamel hypoplasia (E.H) are routinely encountered in primary dentition and early detection and prudent management of the condition facilitates normal occlusal development.
Suzan Sahana +5 more
doaj
This study investigated possible prenatal and neonatal variables that may influence the prevalence of tooth enamel hypoplasia in preterm and low birth weight children (LBW) and a matched control group of term children with normal birth weight (NBW).
Kátia Maria Dmytraczenko Franco +2 more
doaj +1 more source
Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia
Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise +5 more
wiley +1 more source
Localized epidermolysis bullosa simplex with generalized enamel hypoplasia in a child
Epidermolysis bullosa is an uncommon disease characterized by the formation of blisters following minor trauma. The three major types are simplex, junctional, and dystrophic.
GÜNGÖR HATİPOĞLU, MÜJGAN +1 more
core +2 more sources
Assessment of the enamel defects in primary teeth of premature infants
Introduction: The aim of this study was to determine the prevalence of enamel defects in primary dentition of the term and preterm infants.Method and materials: In this historical cohort study, enamel defects (enamel hypoplasia and opacities) were ...
Sh Kakoei, B Bahman Bijari
doaj
Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple +30 more
wiley +1 more source

