Glucose-6-phosphate dehydrogenase deficiency natural history, complications and prognosis
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mahda Alihashemi M.D. [2]
Overview
Overview
The symptoms of G6PD deficiency typically develop after exposure to some foods and medications. Common complications of G6PD deficiency include acute hemolytic anemia and neonatal jaundice.
Natural History, Complications, and Prognosis
Natural History, Complications, and Prognosis
Natural History
- The symptoms of G6PD deficiency typically develop after exposure to some foods and medications.
Complications
- Common complications of G6PD deficiency include:[1]
- Acute hemolytic anemia
- Neonatal jaundice
- Acute kidney failure
Prognosis
- Prognosis is generally good.[2]
References
References
- ↑ Luzzatto L, Nannelli C, Notaro R (April 2016). “Glucose-6-Phosphate Dehydrogenase Deficiency”. Hematol. Oncol. Clin. North Am. 30 (2): 373–93. doi:10.1016/j.hoc.2015.11.006. PMID 27040960.
- ↑ Bubp J, Jen M, Matuszewski K (September 2015). “Caring for Glucose-6-Phosphate Dehydrogenase (G6PD)-Deficient Patients: Implications for Pharmacy”. P T. 40 (9): 572–4. PMC 4571844. PMID 26417175.
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