CPT2 Deficiency: What You Need to Know

Carnitine Palmitoyltransferase II (CPT2) deficiency is a rare genetic disorder that affects the body's ability to use long-chain fats for energy. This can lead to rhabdomyolysis—the breakdown of muscle tissue—especially during stress or illness.

Common Triggers for Rhabdomyolysis

Helpful Resources

Dietary Recommendations

For CPT II deficiency, dietary recommendations primarily focus on reducing the body's reliance on fats for energy. This involves a high-carbohydrate, low-fat, and moderate-protein diet, along with frequent meals to prevent low blood sugar and keep glucose levels stable. For additional detail, see: PMC Article on CPT II Diet.

Emergency Wallet Card

This is an example only. Please consult your doctor to customize this for your specific treatment plan.

Click here to fill out and print your Emergency Wallet Card
Disclaimer: The author of this website is not a doctor. He was diagnosed with CPT2 Deficiency in 1996 and created this site to help others save time. Please consult your physician before making any medical decisions.