Abstract Introduction Gestational hyperthyroidism is an important cause of bone modifications in offspring, resulting from changes in endochondral growth. However, its effect on the craniodental development in offspring is unknown….
Abstract Alexander disease (AxD) is a rare neurodegenerative disorder caused by mutation of the glial fibrillary acidic protein gene. AxD is characterized by severe motor impairment, intellectual disability, epilepsy, megalencephaly,…
Abstract Objective This study aimed to investigate the factors related to the survival of retained deciduous teeth (RDTs). Materials and methods RDTs were identified in panoramic X-ray images in 13,516…
Abstract Infective endocarditis (IE) is a potentially fatal condition caused by bacterial growth on heart valves. Bacteremia-inducing dental procedures are key factors contributing to IE development. Congenital heart disease, the…
Abstract Objectives Systemic and local problems may lead to the disruption of craniofacial growth and development during growth periods. However, no studies have demonstrated the negative effects of the coronavirus…
Abstract Introduction Virtual reality glasses can be used as a distraction method in dental practices for children. This study was carried out to evaluate the effect of virtual reality glasses…
Abstract Dental treatment has been shifted towards more conservative approaches that focus on caries identification at early stage, remineralization of dental surfaces, and preservation of tooth structure. So that, newly…
Abstract In the type III facial growth pattern, craniofacial disharmony is observed, which may be a maxillary retrusion or mandibular advancement as the most diagnosed postures. This case report aims…
Abstract Aim The current study aimed to compare the clinical and radiographic success of potassium nitrate in polycarboxylate cement (KNO 3 /PCA) compared to mineral trioxide aggregate (MTA) in direct…
Abstract Objective Low birthweight infants (LBW) are known to have a significantly high complication rate, and mortality rate, and many of them are admitted to the Neonatal Intensive Care Unit…
Abstract Congenital pain insensitivity syndrome with anhidrosis (CIPA, MIM 256800 ) or hereditary sensory and autonomic neuropathy (HSAN) type IV is a rare autosomal recessive disease. CIPA has characteristic symptoms…
Abstract Burkitt’s lymphoma (BL) is a non-Hodgkin Lymphoma (NHL) type fast growing neoplasm of the B-cells and is one of the most common subtypes of paediatric lymphomas. A case of…
Abstract Background Tooth anomalies may occur during the various developmental stages. Case presentation A 2Y3M-old Japanese girl came to our clinic. At 1Y8M, the mandibular left primary central incisor had…
Abstract Introduction In Japan, the use of general anesthesia for dental treatment (GAD) is common in patients with intellectual disabilities. However, GAD in uncooperative pediatric patients without intellectual disabilities is…
Abstract Background Molar-incisor hypomineralization (MIH) is a qualitative defect in enamel formation with a multifactorial etiology. Studies indicate a high prevalence of MIH across the Americas, yet the prevalence in…
Abstract Introduction In 2018, disease of developmental insufficiency of oral function (DIOF) was added to the Japanese national dental health insurance for typically developing children. We aimed to confirm the…
Abstract Objectives Dental anomalies are often associated with inherited diseases and are frequently seen in the field of pediatric dentistry. Dentin disorders are caused by genetic mutations of genes expressed…
Abstract Objectives Salivary proton Nuclear Magnetic Resonance Spectroscopy ( 1 H NMR) has been widely used in metabonomic studies. A research gap still exists in analysing the metabolic profile in…
Abstract Introduction Down syndrome (DS) is often associated with delayed teeth eruption, gross motor skill acquisition, and feeding difficulties. In typically developing (TD) children, changes in weaning food texture with…
Abstract Objectives Sickle cell anemia (SCA) is the most common inherited disorder around the world. Several studies revealed a low level of serum zinc among sickle patients. However, none of…
