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A rare association - amelogenesis imperfecta, platispondyly and bicytopenia: a case report
INTRODUCTION: Amelogenesis imperfecta is an inherited disease characterized by generalized structural abnormalities of the enamel on all teeth, including both primary and permanent dentition. To the best of our knowledge, this is the first case report of a rare association of amelogenesis imperfecta...
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| Publicado no: | J Med Case Rep |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4624603/ https://ncbi.nlm.nih.gov/pubmed/26511208 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-015-0724-3 |
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