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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Med Case Rep |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2015
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| Θέματα: | |
| Διαθέσιμο Online: | 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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