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...
Sábháilte in:
| Foilsithe in: | J Clin Pathol |
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| Príomhchruthaitheoirí: | , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
BMJ Publishing Group
1996
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| Ábhair: | |
| Rochtain ar líne: | 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 |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
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