Phosphofructokinase deficiency is a genetic disorder; while symptoms can be managed, there is currently no cure
Phosphofructokinase deficiency is a rare genetic disorder affecting muscle metabolism. Treatment focuses on managing symptoms and may include lifestyle modifications.
Metabolic disorder affecting the enzyme phosphofructokinase, leading to impaired energy production in muscles
Muscle weakness, fatigue, cramping, myoglobinuria (presence of myoglobin in the urine)
Genetic testing, clinical evaluation
Variable, depends on the severity of the deficiency
Muscle breakdown, complications affecting energy metabolism
Genetic mutation affecting the PFKM gene
Dietary modifications, supportive care, avoidance of triggers (e.g., intense exercise, fasting)
Dietary modifications, supportive care, avoidance of triggers (e.g., intense exercise, fasting)
Enzyme deficiency affecting glycolysis
Management of symptoms, sometimes dietary adjustments
This information is for general understanding and is not a substitute for professional medical advice. Always consult with healthcare providers for accurate and personalized information related to your health.
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