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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Med Case Rep
Prif Awduron: Laouina, Samir, Chafai El Alaoui, Siham, Amezian, Rachida, Al Bouzidi, Abderrahmane, Sefiani, Abdelaziz., El Alloussi, Mustapha
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2015
Pynciau:
Case Report
Mynediad Ar-lein: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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