The present study aims to investigate the mutation in a Chinese family with dentin dysplasia
type II (DD‐II) and to summarize mutation hotspots, clinical manifestations, and disease …

Objective To provide an evidence-based resource for paleopathologists to consider multiple
skeletal indicators of pathology associated with early tooth loss in children to aid in …

Type II dentinogenesis imperfecta is an autosomal dominant condition that affects dentin
which increases the complexity of the predictability of restorative treatment. Computer‐aided …

Background Various scanning methods aim to reduce intraoral scanner errors, yet no
specific approach targets paediatric patients. Aim Evaluate continuous (C) and …

Rationale: Dentinogenesis imperfecta (DI) is an autosomal-dominant disorder. The most
common clinical manifestations, including obliterated tooth tissues and severe tooth wear …

Children with dentinogenesis imperfecta require restorative or prosthodontic treatment to
minimize the aesthetic and functional impact of the condition. This clinical case report …

İntraoral tarayıcılar (İOS), ağız içi yapıların dijital görüntüsünün hızlı ve doğru bir şekilde
kaydedilmesini sağlayan cihazlardır. İntraoral tarayıcılarla birlikte bilgisayar destekli …

De acordo com Dure-Molla et al. 10 (2015), na DD tipo I ou radicular, os dentes são
clinicamente normais, no entanto, suas raízes são curtas, ocorrendo com frequência …

Background: Computer-engineered complete dentures (CECDs) or digital dentures have
become a popular option for treating completely edentulous patients. CECDs are fabricated …

Introdução: A dentina é um dos principais componentes do dente e encontra-se constituída
por 70% hidroxiapatita, 20% matriz orgânica e 10% água. A dentinogénese é um processo …