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Dentin dysplasia type I

Dentin dysplasia type I is a rare hereditary disturbance of dentin formation characterised clinically by nearly normal appearing crowns and hypermobility of teeth that affects one in every 100 000 individuals and manifests in both primary and permanent dentitions. Radiographic analysis shows obliter...

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Bibliografiska uppgifter
Huvudupphovsmän: Singh, Aarti, Gupta, Sangesh, Yuwanati, Monal Bhaurao, Mhaske, Shubhangi
Materialtyp: Artigo
Språk:Inglês
Publicerad: BMJ Publishing Group 2013
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3702896/
https://ncbi.nlm.nih.gov/pubmed/23814198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-009403
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