Sponsored diagnostic testing programs for Carnitine Palmitoyltransferase II (CPTII or CPT2) Deficiency
Carnitine Palmitoyltransferase II (CPT II) Deficiency is a rare fatty-acid oxidation disorder that limits the body’s ability to produce energy during fasting or physical stress. It commonly causes episodes of muscle pain, weakness, or rhabdomyolysis after exercise, illness, or prolonged fasting, with severity ranging from exercise-induced symptoms to serious infantile forms with multisystem involvement.
1 program found for Carnitine Palmitoyltransferase II (CPTII or CPT2) Deficiency
The Invitae Unlock™ Cardiomyopathy & Arrhythmia program offers no-charge genetic testing for U.S. patients with suspected inherited cardiomyopathy or arrhythmia. The comprehensive panel supports diagnostic clarification, risk assessment, and family variant identification. Eligible patients may access testing at no cost when ordered by a qualified healthcare provider.
