Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

Barron, Martin; McDonnell, Sinéad; C Mackie, I; J. Dixon, Michael

doi:10.1186/1750-1172-3-31

Public

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

Published in Orphanet Journal of Rare Diseases • Nov 20, 2008

Authors:

Martin Barron

Sinéad McDonnell

I C Mackie

Abstract

The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an in...

Subject

Dentinogenesis imperfecta

Medicine

Amelogenesis imperfecta

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