Carnitine palmitoyl transferase II deficiency, severe infantile form

The severe infantile form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the early-onset form of the disease.

Also known as: CPT II deficiency, infantile, CPT2, hepatocardiomuscular form, CPT2, severe infantile form, CPTII, hepatocardiomuscular form, CPTII, severe infantile form, Carnitine palmitoyl transferase II deficiency, hepatocardiomuscular form, Carnitine palmitoyl transferase deficiency type 2, hepatocardiomuscular form, Carnitine palmitoyl transferase deficiency type 2, severe infantile form

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