Diagnostic features and pedodontic-orthodontic management in dentinogenesis imperfecta type II: a case report

Autor:	K. Ch. Huth, Ekaterini Paschos, Reinhard Hickel, T. Sagner
Rok vydání:	2002
Předmět:	Orthodontics business.industry Dentinogenesis imperfecta Permanent dentition Follow up studies Autosomal dominant trait Opalescent dentin Dentistry medicine.disease stomatognathic diseases stomatognathic system Medicine Differential diagnosis business General Dentistry
Zdroj:	International Journal of Paediatric Dentistry. 12:316-321
ISSN:	1365-263X 0960-7439
Popis:	Dentinogenesis imperfecta type II, also known as hereditary opalescent dentin, is an isolated inherited condition transmitted as an autosomal dominant trait affecting the primary and permanent dentition. The combined pedodontic-orthodontic management of a 4-year-old child is described. Following orthodontic analysis to encourage a favourable growth outcome, treatment comprised restoration of the primary teeth with stainless steel crowns and composite crowns. Differential diagnosis and alternative therapies, including orthodontic considerations, are discussed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::103211ab96e301ce62d48aa0067d0305 https://doi.org/10.1046/j.1365-263x.2002.00390.x Zobrazit plný text záznamu Plný text