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Glucose-6-Phosphate Dehydrogenase (G6PD). - Coggle Diagram
Glucose-6-Phosphate Dehydrogenase (G6PD).
DEFINITION
.
a genetic disorder that affect RBC and may contribute to anemia. the severe form of the deficiency is called favism, which causes more symptoms and poses more risks than other types of G6PD deficiency
CAUSES
inherited
because it was passed down in genes from one or both of the parents. The gene responsible for this condition is on the X chromosome
SIGN & SYMPTOM
shortness of breath
tachycardia
urine that is dark/yellow-orange
paleness
fatigue
jaundice
enlarged spleen
INVESTIGATION
complete blood count
serum hemoglobin
reticulocyte count
TREATMENT
blood transfusion
give oxygen
Avoiding certain medicines, foods, and environmental exposures
Telling your providers that you have G6PD deficiency
Checking with your provider before taking any medicine