Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity

Fanconi anemia is a recessive genetic disorder with a wide range of presenting symptoms, from multiple congenital defects to exclusively (pan) cytopenia. Scapula alata may be a rare symptom of FA.

Detalles Bibliográficos
Autores principales: van Adrichem, Renee, de Weger, Vincent, Broere, Daniel, van Herrewegen, Femke, Amaya, Jeremy, ten Tusscher, Gavin William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745367/
https://www.ncbi.nlm.nih.gov/pubmed/31534721
http://dx.doi.org/10.1002/ccr3.2323

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745367/
https://www.ncbi.nlm.nih.gov/pubmed/31534721
http://dx.doi.org/10.1002/ccr3.2323

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