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==reference value/cut-off of Hb==
*adjust according to altitude of living
==diagnosis==
*POC test kit: HemoCue
*ferritin increases in inflammation in order to deliver more iron stimulated by inflammation itself as well as to avoid pathogens try to consume iron
*serum transferrin (TIBC) increases in IDA, decreases in inflammation
*zinc protoporphyrin (Zpp)
*soluble transferrin receptor (sTfr)
==cause==
*malaria does not cause IDA directly; destruction of RBCs by ''Plasmodium'' does not cause iron loss
**anemia by malaria is mainly by inflammation, which suppresses iron absorption
 
==sickle cell anemia==
*monogenetic recessive disorder
*hemoglobin mutation
*HbA mutated into HbS (sickle cell trait) or HbC (West Africa)
*sickle cell trait protect against death from severe malaria
**not prevent infection itself
 
===clinical picture of SCD===
*affects all organ systems
*disease pattern and severity varies very much on patients
 
===chronic management===
*first to identify high risk groups
 
==thalassemia==
*decreased hemoglobin production
**sickle cell trait is problem of hemoglobin destruction
*beta thalassemia affects beta chain of hemoglobin
*alpha thalassemia affects alpha chain of hemoglobin
*major, media, minor

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