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Up to: Carnitine palmitoyltransferase II deficiency
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.
This condition has no sub-types.