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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Pubblicato in:	J Clin Pathol
Autori principali:	Zaidi, Y, Sivakumaran, M, Graham, C, Hutchinson, R M
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	BMJ Publishing Group 1996
Soggetti:	Research Article
Accesso online:	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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