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10.11604/pamj.2014.19.310.5576

http://scihub22266oqcxt.onion/10.11604/pamj.2014.19.310.5576
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C4394002!4394002!25883737
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suck abstract from ncbi


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pmid25883737      Pan+Afr+Med+J 2014 ; 19 (ä): ä
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  • Hyper-reactive Malarial Splenomegaly (HMS) in a patient with ? thalassaemia syndrome #MMPMID25883737
  • Amoako YA; Bedu-Addo G
  • Pan Afr Med J 2014[]; 19 (ä): ä PMID25883737show ga
  • This report describes a case of hyper-reactive malarial splenomegaly in a patient with a thalassaemia syndrome. Increased haemoglobin A2 is valuable for the diagnosis of common forms of ?-thalassemia, while haemoglobin F (HbF) helps in diagnosis of the rarer ??- forms. Thalassemia is characterised by splenomegaly and is common in malaria endemic areas. Hyper-reactive malarial splenomegaly is also a common cause of massive splenomegaly in malaria endemic areas. Splenic enlargement regresses with prolonged antimalarial therapy
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