Dentinogenesis Imperfecta type II (DI2), also known as hereditary opalescent dentin, is one
of the most common genetic disorders affecting the structure of dentin, not related with …

A 20-year-old woman presented with an unesthetic appearance and severe wear of the
anterior teeth. Definitive expected treatment was designed by multidisciplinary combination …

Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal
dominant mutation in dentin sialophosphoprotein gene. Defective dentin development …

Dentinogenesis imperfecta (DI) is a hereditary condition that may affect both primary and
permanent dentition and is characterized by abnormal dentin formation. The teeth may be …

BACKGROUND: Dentinogenesis imperfecta is one of the most common hereditary disorders
of dentine formation. Opalescent teeth composed of irregularly formed and undemineralised …

Vyas Dental College & Hospital, India Abstract-Dentinogenesis imperfecta is a
developmental disorder affecting the structure of the teeth. Both deciduous and permanent …

Objectives The aim of this study was to investigate the wear behavior of Dentinogenesis
imperfecta type II (DGI-II) dentin and elucidate the correlation between its tribological …

Dentinogenesis imperfect is a hereditary dentin defect leading to discoloration as well as
early tooth wear. Timely diagnosis and treatment are required to prevent further tooth loss …

A dentinogénese é um processo altamente controlado que resulta na transformação
paulatina de um tecido não mineralizado numa matriz mineralizada. Interferências na fase …

Dental hard tissue is subject to variety of disorders. Dentinogenesis Imperfecta is one such
disorder attributed to heredity. It is known to be an autosomal dominant trait. Teeth with such …