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Dentin dysplasia type I—novel findings in deciduous and permanent teeth
BACKGROUND: Dentin dysplasia type I (DD-I) is a rare autosomal dominant hereditary disorder which seriously affects the root development of teeth, causing spontaneous tooth loss (in teenagers). At present, the study of DD-I focuses on familial and phenotypic analyses and reports regarding the ultras...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689058/ https://www.ncbi.nlm.nih.gov/pubmed/26693824 http://dx.doi.org/10.1186/s12903-015-0149-9 |