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Hyper-reactive Malarial Splenomegaly (HMS) in a patient with β thalassaemia syndrome
This report describes a case of hyper-reactive malarial splenomegaly in a patient with a thalassaemia syndrome. Increased haemoglobin A(2) is valuable for the diagnosis of common forms of β-thalassemia, while haemoglobin F (HbF) helps in diagnosis of the rarer δβ- forms. Thalassemia is characterised...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394002/ https://www.ncbi.nlm.nih.gov/pubmed/25883737 http://dx.doi.org/10.11604/pamj.2014.19.310.5576 |