Autosomal recessiv
En arvelig sygdom i mitokondriernes oxidation af langkædede fedtsyrer med varierende forløb, herunder kardiomyopati, hypoketotisk hypoglykæmi, leversygdom, nedsat træningstolerance og rhabdomyolyse.
Analyserede gener
Også kendt som
ACADVLD; very long-chain acyl-CoA dehydrogenase deficiency; acyl-CoA dehydrogenase, very long-chain, deficiency OF; Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD); very long-chain acyl-Coenzyme A dehydrogenase deficiency; VLCAD; VLCAD deficiency; VLCADD
