The diagnosis and treatment of dyskeratosis congenita: a review

Dyskeratosis congenita (DC) is an inherited bone marrow failure (BMF) syndrome characterized by the classic triad of abnormal skin pigmentation, nail dystrophy, and oral leukoplakia. However, patients usually develop BMF and are predisposed to cancer, with increased risk for squamous cell carcinoma...

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Detalles Bibliográficos
Autores principales: Fernández García, M Soledad, Teruya-Feldstein, Julie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145822/
https://www.ncbi.nlm.nih.gov/pubmed/25170286
http://dx.doi.org/10.2147/JBM.S47437

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145822/
https://www.ncbi.nlm.nih.gov/pubmed/25170286
http://dx.doi.org/10.2147/JBM.S47437

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