Type I Dentin Dysplasia: The Literature Review and Case Report of a Family Affected by Misrecognition and Late Diagnosis

Background and Objectives: Type I dentin dysplasia (DD-I) is a rare genetic disorder with autosomal dominant or recessive inheritance at risk of late or long-misunderstood diagnosis because the teeth, compared to other degenerative dentin diseases, do not have coronal defects and/or alterations but...

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Detalles Bibliográficos
Autores principales: Putrino, Alessandra, Caputo, Martina, Galeotti, Angela, Marinelli, Enrico, Zaami, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456812/
https://www.ncbi.nlm.nih.gov/pubmed/37629767
http://dx.doi.org/10.3390/medicina59081477

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456812/
https://www.ncbi.nlm.nih.gov/pubmed/37629767
http://dx.doi.org/10.3390/medicina59081477

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