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Systemic Mastocytosis: Predominantly Involving the Bone, A Case Report
Systemic mastocytosis (SM) is a rare clonal disorder of mast cells that can range from chronic smouldering type to aggressive mast cell leukaemia. It presents with non–specific symptoms like urticaria pigmentosa, unexplained flushing, hypotension and abdominal cramps, which may lead to a misdiagnosi...
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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
JCDR Research and Publications (P) Limited
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3843398/ https://ncbi.nlm.nih.gov/pubmed/24298498 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2013/5669.3493 |
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