Fatal bone marrow embolism in a patient with sickle cell beta + thalassaemia.
Sickle cell beta + thalassaemia is regarded as the mildest of the sickle cell haemoglobinopathy syndromes with a benign natural course. In contrast to sickle cell disease, severe life threatening complications are not usually associated with this genotype. A case of a 30 year old West Indian man who...
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| Vydáno v: | J Clin Pathol |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
1996
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC500734/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9038769/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jcp.49.9.774 |
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