Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review
Dentinogenesis imperfecta is an autosomal dominant genetic disorder with abnormal dentin structure affecting both primary and permanent dentitions leading to discolouration and attrition of teeth. Diagnosis is usually based on family history, a detailed clinical examination and pedigree construction...
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| Autores principales: | , , , |
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| Lenguaje: | English |
| Publicado: |
Universidad de La Frontera. Facultad de Medicina
2012
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| Acceso en línea: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000200018 |
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