Dentinogenesis imperfecta (DI) and amelogenesis imperfecta (AI) are hereditary
abnormalities of dental hard tissues. Dental abnormalities may also be accompanied by …

Amelogenesis imperfecta (AI) is a rare genetic disorder affecting children and adults.
Knowledge about AI is limited to clinical representation and radiographical findings. Various …

Taurodontism is a continuous anatomical variation of permanent and primary posterior teeth
represented by an enlargement of the pulp cavity. A high prevalence of the trait is reported in …

Periodontal disease is the most common medical condition in small animal veterinary
patients. The earlier onset of periodontal disease is due primarily to the popularity of small …

牙釉质发育不全是一种牙齿在发育过程中受到遗传或环境因素影响而导致牙釉质形成或矿化
障碍的疾病, 可导致患牙颜色异常, 结构缺损, 患者表现出牙齿变色, 牙齿敏感 …

Amelogenesis imperfecta is a collection of genetic disorders that impair the structure of
dental enamel. The condition presents in a variety of ways, affecting enamel development …

Bone growth requires a balance of minerals such as calcium, phosphorus, and factors of
bone biomineralization. The difference between jaws' bones and the rest of the bones is the …

Introdução: A amelogênese imperfeita faz parte de um grupo de condições que
comprometem clínica e estruturalmente o esmalte dentário. O tipo de defeito associado com …

Amelogenesis imperfecta (AI), dentinogenesis imperfecta (DI), and dentin dysplasia (DD)
are hereditary illnesses that affect the growth and architecture of teeth's hard tissues …

Objectives: To assess the management strategies for treating deciduous and young
permanent teeth with Developmental defects of enamel (DDE) presenting post-eruptive …