Carnitine Palmitoyltransferase II (CPTII or CPT2) Deficiency

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

Programs

1 program
Invitae Unlock™

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

The Invitae Unlock™ Cardiomyopathy & Arrhythmia program offers sponsored genetic testing for U.S. patients with suspected inherited cardiomyopathy or arrhythmia. The comprehensive panel supports diagnostic clarification, risk assessment, and family variant identification. The test is billed to insurance first; when a claim is denied or the patient is uninsured, the program's sponsor covers the cost of testing. Testing must be ordered by a qualified healthcare provider.

Cardiology
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Performing lab
Invitae | Labcorp