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1.
J Clin Pediatr Dent ; 43(3): 147-154, 2019.
Article in English | MEDLINE | ID: mdl-30964718

ABSTRACT

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 osteogenesis imperfecta, which involves both primary and permanent dentitions. The purpose of this article is to perform a scoping review of the published peer-reviewed literature (1986-2017) on DI2 management in children and to outline the most relevant clinical findings extracted from this review. Forty four articles were included in the present scoping review. According to the extracted data, the following are the most important tasks to be performed in clinical pediatric dentistry: to re-establish the oral mastication, esthetics, and speech, and the development of vertical growth of alveolar bone and facial muscles; to reduce the tendency to develop caries, periapical lesions and pain; to preserve vitality, form, and size of the dentition; to avoid interfering with the eruption process of permanent teeth; to decrease the risk of tooth fractures and occlusion disturbances; to return the facial profile to a more normal appearance; and to prevent or treat possible temporomandibular joint problems. Therefore, Pediatric Dentists should bear in mind that early diagnosis and treatment, together a long-term follow-up of DI2 in children, continue to be the best approaches for achieving enhanced patient psychological well-being and, in consequence, their quality of life.


Subject(s)
Dental Care for Children , Dentinogenesis Imperfecta , Child , Child, Preschool , Dental Care for Children/methods , Dental Care for Children/psychology , Dentinogenesis Imperfecta/psychology , Dentinogenesis Imperfecta/therapy , Dentition, Permanent , Esthetics, Dental , Humans , Quality of Life
2.
Dent Update ; 37(6): 364-6, 369-71, 2010.
Article in English | MEDLINE | ID: mdl-20929150

ABSTRACT

UNLABELLED: Dentinogenesis imperfecta (DI) is a hereditary condition which affects the development of dentine in both the primary and permanent dentitions. Three types of DI have been described in the literature. The presentation of DI is variable, depending on the type and severity of the disease. Early intervention in the treatment of a patient with DI is extremely important both for psycho-social and for functional reasons. This paper attempts to describe the clinical presentation and management of DI, and explores its association with certain medical conditions. CLINICAL RELEVANCE: Recognition of DI is important, so that correct treatment principles may be instituted.


Subject(s)
Dentinogenesis Imperfecta/therapy , Child , Crowns , Dental Bonding , Dental Veneers , Dentin/abnormalities , Dentin/pathology , Dentinogenesis Imperfecta/classification , Dentinogenesis Imperfecta/psychology , Denture, Overlay , Early Diagnosis , Female , Humans , Male , Osteogenesis Imperfecta/complications , Root Canal Therapy , Self Concept , Vertical Dimension
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