Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report

BACKGROUND: Amelogenesis imperfecta represents a group of developmental conditions, clinically and genetically heterogeneous, that affect the structure and clinical appearance of enamel. Amelogenesis imperfecta occurred as an isolated trait or as part of a genetic syndrome. Recently, disease-causing...

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Detalles Bibliográficos
Autores principales: Cherkaoui Jaouad, Imane, El Alloussi, Mustapha, Chafai El alaoui, Siham, Laarabi, Fatima Zahra, Lyahyai, Jaber, Sefiani, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327795/
https://www.ncbi.nlm.nih.gov/pubmed/25636655
http://dx.doi.org/10.1186/1472-6831-15-14

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327795/
https://www.ncbi.nlm.nih.gov/pubmed/25636655
http://dx.doi.org/10.1186/1472-6831-15-14

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