Also Known As
CPT II deficiency, myopathic, stress-inducedCPT2, adult-onset formCPT2, myopathic formCPTII, adult-onset formCPTII, myopathic formCarnitine palmitoyl transferase II deficiency, adult-onset formCarnitine palmitoyl transferase deficiency type 2, adult-onset formCarnitine palmitoyl transferase deficiency type 2, myopathic formcarnitine palmitoyl transferase II deficiency, myopathic formCARNITINE PALMITOYLTRANSFERASE II deficiency, late-onsetCARNITINE PALMITOYLTRANSFERASE II deficiency, myopathic, stress-inducedCPT 2 deficiency, myopathicCarnitine Palmitoyltransferase 2 deficiency, adult-onsetCarnitine Palmitoyltransferase 2 deficiency, myopathicCarnitine Palmitoyltransferase 2 deficiency, myopathic, stress-inducedCpt2 deficiency, late-onset
Definition
The myopathic form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited metabolic disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the most common and the least severe form of CPT II deficiency.