Also called: Glucose-6-phosphate dehydrogenase deficiency
Important: This page is general information, not medical advice. It does not recommend or prescribe any treatment. Always consult your doctor or pharmacist before starting, stopping or changing any medicine.
About G6PD Deficiency
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.
It sits within Genetics/Birth Defects.
When to speak to someone. Reading about a topic cannot tell you whether it applies to you. Speak to a doctor or pharmacist if symptoms are severe, sudden, getting worse, or simply not going away — and seek emergency care immediately for chest pain, breathing difficulty, sudden weakness or confusion, or a serious allergic reaction.
Research on G6PD Deficiency
59 studies areregistered for this condition on ClinicalTrials.gov, the U.S. National Library of Medicine's public registry. A selection is below — the links go straight to the registry entry, not to a summary of ours.
What a registered study does and does not mean. Registration means a study exists and has been declared publicly. It says nothing about whether the treatment being tested works, is safe, or is available to you. Many studies find no benefit — that is what research is for. Never seek out an experimental treatment on the strength of a registry entry alone.
Research currently under way
- Early Check: Expanded Screening in NewbornsRTI International
- High-Dose Vitamin C in G6PDA and Pyruvate Kinase Deficiency: A Safety StudyUniversity of Utah
- The Efficacy of Ursodeoxycholic Acid (UDCA) as Adjuvant Therapy to Phototherapy in the Management of Neonatal Indirect HyperbilirubinemiaTishreen University Hospital
- Serological Testing and Treatment for Plasmodium Vivax Malaria: a Trial in Ethiopia and MadagascarLondon School of Hygiene and Tropical Medicine
- Primaquine for Vivax Malaria in G6PD Intermediate and Deficient Cases.Menzies School of Health Research
- Screening of Coexistence Between Sickle Cell Anaemia and G6PD DeficiencyFatma Hussein Mahmoud
Research already completed
- Short Course Primaquine for the Radical Cure of P. Vivax - Papua New GuineaMacfarlane Burnet Institute for Medical Research and Public Health Ltd
- Radical Cure (RC) With Tafenoquine or Primaquine After Semi-quantitative G6PD Testing: A Feasibility Study in PeruMedicines for Malaria Venture
- Short Course Primaquine for the Radical Cure of P. Vivax Malaria - IndonesiaMenzies School of Health Research
- Baby Detect : Genomic Newborn ScreeningCentre Hospitalier Universitaire de Liege
- Use of Macrolides in Acute Chest Syndrome: A Multicenter Retrospective StudyCentre Hospitalier de Saint-Denis
- Safety and Efficacy of Different Regimens of Primaquine on Vivax Malaria Treatment in G6PD Deficient PatientsFundação de Medicina Tropical Dr. Heitor Vieira Dourado
Study data from ClinicalTrials.gov, a service of the U.S. National Library of Medicine. Retrieved 2026-07-30. Registry entries are supplied by study sponsors and investigators; ClinicalTrials.gov does not verify their scientific validity. PocketsInfo is not affiliated with, and not endorsed by, the NLM or the NIH.
Where to read more
Rather than paraphrase, we point you to the primary sources. Every link below is to a government health agency, a national institute or a recognised medical body — grouped by what you are trying to find out.
Learn More
- Anemia, Nonspherocytic Hemolytic, Due to G6PD DeficiencyGenetic and Rare Diseases Information Center
- Blood Count Tests: MedlinePlus Health TopicNational Library of Medicine
- G6PD Deficiency (For Parents)Nemours Foundation
- G6PD TestNational Library of Medicine
- Glucose-6-phosphate dehydrogenase deficiencyMedical Encyclopedia
Genetics
- Glucose-6-phosphate dehydrogenase deficiency: MedlinePlus GeneticsNational Library of Medicine
Clinical Trials
- ClinicalTrials.gov: Glucosephosphate Dehydrogenase DeficiencyNational Institutes of Health
Medical subject headings
Clinicians and researchers index this subject under Glucosephosphate Dehydrogenase Deficiency. These are the terms to use when searching medical literature.
This page is built from the MedlinePlus health topic record for G6PD Deficiency, a service of the U.S. National Library of Medicine (NLM), National Institutes of Health. Information is from MedlinePlus.gov. PocketsInfo is not affiliated with, and is not endorsed by, the NLM or the NIH. Retrieved 30 July 2026.