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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Detalles Bibliográficos
Autores principales: Laouina, Samir, Chafai El Alaoui, Siham, Amezian, Rachida, Al Bouzidi, Abderrahmane, Sefiani, Abdelaziz., El Alloussi, Mustapha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624603/
https://www.ncbi.nlm.nih.gov/pubmed/26511208
http://dx.doi.org/10.1186/s13256-015-0724-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624603/
https://www.ncbi.nlm.nih.gov/pubmed/26511208
http://dx.doi.org/10.1186/s13256-015-0724-3

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