Pyruvate kinase deficiency
| Pyruvate kinase deficiency | |
|---|---|
| Other names | Erythrocyte pyruvate kinase deficiency | 
| Phosphoenolpyruvate | |
| Specialty | Hematology | 
| Symptoms | Anemia, tachycardia | 
| Causes | Mutation in PKLR gene | 
| Diagnostic method | Physical exam, CBC | 
| Treatment | Blood transfusion | 
Pyruvate kinase deficiency is an inherited metabolic disorder of the enzyme pyruvate kinase which affects the survival of red blood cells. Both autosomal dominant and recessive inheritance have been observed with the disorder; classically, and more commonly, the inheritance is autosomal recessive. Pyruvate kinase deficiency is the second most common cause of enzyme-deficient hemolytic anemia, following G6PD deficiency.