G6PD Deficiency

Summary

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder that is most common in males. About 1 in 10 African American males in the United States has it. G6PD deficiency mainly affects red blood cells, which carry oxygen from the lungs to tissues throughout the body. The most common medical problem it can cause is hemolytic anemia. That happens when red blood cells are destroyed faster than the body can replace them.

If you have G6PD deficiency, you may not have symptoms. Symptoms happen if your red blood cells are exposed to certain chemicals in food or medicine, certain bacterial or viral infections, or stress. They may include:

• Paleness
• Jaundice
• Dark urine
• Fatigue
• Shortness of breath
• Enlarged spleen
• Rapid heart rate

A blood test can tell if you have it. Treatments include medicines to treat infection, avoiding substances that cause the problem with red blood cells, and sometimes transfusions.

NIH: National Library of Medicine

Learn More

• Blood Count Tests: MedlinePlus Health Topic National Library of Medicine
• Class I Glucose-6-Phosphate Dehydrogenase Deficiency Genetic and Rare Diseases Information Center
• G6PD Deficiency (Glucose-6-Phosphate Dehydrogenase) (For Parents) Nemours Foundation
• G6PD Test National Library of Medicine
• Glucose-6-phosphate dehydrogenase deficiency Medical Encyclopedia

Clinical Trials

• ClinicalTrials.gov: Glucosephosphate Dehydrogenase Deficiency National Institutes of Health

Patient Handouts

• Glucose-6-phosphate dehydrogenase Medical Encyclopedia

Genetics

• Glucose-6-phosphate dehydrogenase deficiency: MedlinePlus Genetics National Library of Medicine

Journal Articles

• G6PD Deficiency