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Hunter syndrome with persistent thrombocytopenia
A case of Hunter syndrome, 6½-year-old boy presented with persistent thrombocytopenia and bleeding diathesis. However, cytopenia is not a usual presentation in patients with mucopolysaccharidosis II. After ruling out other causes of severe thrombocytopenia, a clinical possibility of chronic Epstein-...
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| Veröffentlicht in: | BMJ Case Rep |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Publishing Group
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6506028/ https://ncbi.nlm.nih.gov/pubmed/31005860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2018-226518 |
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