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Dentinogenesis imperfecta type II: A case report with 17 years of follow-up
Dentinogenesis imperfecta is a dominant autosomal hereditary disorder of dentin formation that affects the deciduous and permanent teeth. Its etiology is characterized by inadequate cell differentiation during odontogenesis. The clinical characteristics of dentinogenesis imperfecta are discolored te...
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| Pubblicato in: | Imaging Sci Dent |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Korean Academy of Oral and Maxillofacial Radiology
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5489669/ https://ncbi.nlm.nih.gov/pubmed/28680850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5624/isd.2017.47.2.129 |
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