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G6PD Deficiency
A hereditary enzyme disorder that makes red blood cells (RBCs) vulnerable to oxidative damage
X-linked recessive
The genetic etiology of G6PD, explaining why it is more common in males
NADPH
Produced via the pentose phosphate pathway, this substance helps maintain glutathione
Glutathione
The substance that protects RBCs from oxidative stress; it decreases when NADPH is low
Hemolysis
The destruction of RBCs that occurs when G6PD-deficient cells are exposed to triggers
Fava beans
The food trigger most well-known for causing hemolysis, leading to a condition called favism
Infections
Identified as the most common trigger for a hemolytic episode in G6PD
Naphthalene
A chemical found in mothballs that acts as a trigger for hemolysis
Darker urine color
A clinical manifestation of a hemolytic crisis, often seen with jaundice (yellow of the white eyes)
Folate (Folic Acid)
A micronutrient often recommended in chronic hemolysis to support RBC production
Antioxidants (Vitamin C & E)
Supplements that may help reduce oxidative stress, though intake should be moderate
Hydration
This is critical during hemolytic episodes to help prevent kidney complications
Bilirubin excretion
In G6PD newborns, early feeding is promoted specifically to encourage this