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

Abstract:

: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.

journal_name

Int J Paediatr Dent

authors

Huth KCh,Paschos E,Sagner T,Hickel R

doi

10.1046/j.1365-263x.2002.00390.x

subject

Has Abstract

pub_date

2002-09-01 00:00:00

pages

316-21

issue

5

eissn

0960-7439

issn

1365-263X

pii

390

journal_volume

12

pub_type

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