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Generalised hypomineralisation of enamel in oculodentodigital dysplasia: comprehensive dental management of a case
Oculodentodigital dysplasia (ODDD) is a rare congenital disorder characterised by developmental abnormalities of the eye, dentition and digits of the hands and feet, with neurological symptoms reported in 30% of individuals. Dental anomalies associated with ODDD include enamel hypoplasia and subsequ...
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| Publicado no: | BMJ Case Rep |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7802714/ https://ncbi.nlm.nih.gov/pubmed/33431460 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-238079 |
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