Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations

Fanconi anemia is a recessive disorder associated with chromosomal instability. It is marked by phenotypical heterogeneity which includes medullary deficiency, a variable malformation syndrome, a predisposition to develop acute leukaemias myéloïdes (ALM) and a cellular over-sensitiveness with the ag...

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Detalles Bibliográficos
Autores principales: Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, Otmani, Ihssane El, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011001/
https://www.ncbi.nlm.nih.gov/pubmed/29942418
http://dx.doi.org/10.11604/pamj.2017.28.286.4372

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011001/
https://www.ncbi.nlm.nih.gov/pubmed/29942418
http://dx.doi.org/10.11604/pamj.2017.28.286.4372

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