Carnitine palmitoyl transferase II deficiency, myopathic form

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.

Also known as: CPT II deficiency, myopathic, stress-induced, CPT2, adult-onset form, CPT2, myopathic form, CPTII, adult-onset form, CPTII, myopathic form, Carnitine palmitoyl transferase II deficiency, adult-onset form, Carnitine palmitoyl transferase deficiency type 2, adult-onset form, Carnitine palmitoyl transferase deficiency type 2, myopathic form

0 clinical trials for this condition and its sub-types, 0 tagged with Carnitine palmitoyl transferase II deficiency, myopathic form itself.