Agenesis of bilateral maxillary canines is very rare and mesiodens is a commonly occurring supernumerary tooth type. Concomitant occurrence of both hypodontia and hyperdontia is extremely rare and it is a condition of mixed numeric variation in the same individual. The reported prevalence of this condition ranges between 0.002% and 3.1%. The purpose of this case report is to describe a rare occ...

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 associated with a few syndromes. a 9-year-old girl with minor thalassemia referred to the department of pediatric dentistry of the mashhad faculty ...

root canal anatomy diversity and aberrations are common especially in permanent dentition. a thorough understanding of the basic root canal anatomy and its diversities are necessary for successful endodontic treatment. mandibular second premolars are usually single-rooted and have one root canal. incidence of three separate root canals in this tooth is quite rare and taurodontism with three sep...

Amelogenesis Imperfecta (AI) is a hereditary enamel defect which is characterized by developmental abnormalities in the quantity and/ or quality of enamel. This condition has been associated with dental anomalies, including taurodontism, congenitally missing teeth, delayed eruption, crown resorption, pulpal calcifications and odontogenic fibromas. This paper presents two cases of AI which were ...

Case report Clinical, radiological and genetic findings revealed common features of Goltz-Gorlin syndrome and pure ED. Oro-dental characteristics of the patient mostly corresponded to those described in the literature. However, previously unreported oro-dental findings such as taurodontism, peg-shaped teeth and microdontia are considered unusual for Goltz-Gorlin syndrome, but similar to the den...

Dentinal dysplasia type I (DDI) is a rare disturbance in dentin formation. This case report illustrates different radiographic features from other reported DDI cases in that only one quadrant (lower right posterior teeth) has the characteristic of DDI and both right and left upper molars exhibit taurodontism. This finding might be a variation of DDI. However, it is possible that this type of de...

Tel: +98 21 84902473 Fax: +98 21 84902473 Email: [email protected] Klinefelter syndrome includes a group of chromosomal disorders with at least one additional X chromosome in male karyotype (46,XY). Up to now, different dental manifestations such as taurodontism, congenital absence of permanent teeth, shovel incisors, occlusal anomalies and increased permanent tooth size have been reported...

OBJECTIVE Hypophosphatemic rickets is an uncommon metabolic bone disorder which affects all ages and both sexes. It is characterized by low concentration of serum phosphate levels, impairment of mineralization of bone matrix and teeth with variable etiology. Dental problems in this disorder have not been described well in previous studies. METHODS All hypophosphatemic rickets patients who cam...

INTRODUCTION Dental anomalies (DAs) are the result of disorders that are able to modify the shape, number, size, and structure of teeth. This study aimed to evaluate the prevalence of DAs using panoramic radiographs in a population of the City of Belém, northern Brazil. MATERIALS AND METHODS In this study, 487 panoramic radiographs were evaluated searching for DAs. Dental records were reviewe...

Case report A 3-year-old boy was seen at the Department of Maxillo-Facial Surgery and Paediatric Dentistry of the Children’s Hospital of Trieste. The multi-systemic features of XLPDR included a number of oro-dental manifestations such as misshapen teeth, scissor bite, swallowing difficulties, agenesis of the 4 permanent second premolars, taurodontism, early resorption of deciduous roots, and pr...