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A rare case of Wiskott-Aldrich Syndrome with normal platelet size: a case report
BACKGROUND: Wiskott-Aldrich syndrome is a rare X-linked disorder characterized by microthrombocytopenia, eczema, and recurrent infections. It is caused by mutations of the WAS gene. Microthrombocytopenia has been regarded as the key criteria in diagnosing this rare condition. However, in this case r...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928304/ https://www.ncbi.nlm.nih.gov/pubmed/27356510 http://dx.doi.org/10.1186/s13256-016-0944-1 |