載入...
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...
Na minha lista:
| 發表在: | BMJ Case Rep |
|---|---|
| 主要作者: | |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BMJ Publishing Group
2021
|
| 主題: | |
| 在線閱讀: | 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 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|