LCHAD
Engelske synonym: LCHAD deficiency,LCHADD,Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Definisjon
A mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood of hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and, frequently, cardiac involvement with arrhythmias and/or cardiomyopathy.
Fra Orphanet
ORPHA: 5
Klassifiseringsnivå: Disorder
ICD-10: E71.3