Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:1.3.1.8 (
acyl-CoA dehydrogenase
)
785
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Fatty acid oxidation defects
can cause recurrent rhabdomyolysis or chronic progressive muscle weakness. Diagnosis is often possible on blood using tandem mass spectrometry or molecular genetic techniques. Riboflavin and carnitine are effective in some cases of multiple
acyl-CoA dehydrogenase
deficiency and primary carnitine deficiency, respectively. Controlled trials are needed to evaluate other proposed forms of treatment.
...
PMID:Fatty acid oxidation defects in muscle. 984 98
