G6PD Deficiency is when someone doesn't have enough of the enzyme G6PD, which protects red blood cells. It mainly affects red blood cells, which
carry oxygen from the lungs to tissues throughout the body. The most common early detection for this is Newborn Screening after 24hrs of life after birth. G6PD is a
genetic disorder that
occurs most often in males.
Medical problem associated with glucose-6-phosphate dehydrogenase deficiency:
- Hemolytic Anemia. Occurs when red blood cells are destroyed faster than the body can replace them. Manifestation of this problem is yellowing of the skin and whites of the eyes (jaundice), dark urine, fatigue, shortness of breath, and a rapid heart rate.
- Mild to severe jaundice in newborns. Many people with this disorder, however, never experience any signs or symptoms.
How common is G6PD? An estimated 400 million people worldwide have glucose-6-phosphate
dehydrogenase deficiency. Mostly occurs in certain parts of Africa, Asia and Mediterranean.
- ANTIBIOTICS
Trimethoprin
Sulfamethoxazole
Nalidixic Acid
Chloramphenicol
Nitrofurantoin
Antimalarials; Primaquine, Chloroquine, Quinacrine
- CHEMICALS
Naphthalene
- OTHERS
Vitamin K analogs
Methylene Blue
Probenecid
Acetylsalicylic Acid (e.g. aspirin, aspilet)
Phenazopyridine
- ILLNESSES
Hepatitis
Sepsis
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G6PD drugs to Avoid