- LCAD deficiency
- LCAD de·fi·cien·cy long-chain acyl-CoA dehydrogenase deficiency; see under acyl-CoA dehydrogenase.
Medical dictionary. 2011.
LCAD deficiency
Look at other dictionaries:
long-chain acyl-CoA dehydrogenase (LCAD) deficiency — a defect in mitochondrial beta oxidation due to a mutation in the gene (locus: 2q34 q35) encoding the acyl CoA dehydrogenase that acts on long chain length fatty acids. It is clinically similar to MCAD deficiency, but urinary excretion is of long … Medical dictionary
Medium-chain acyl-coenzyme A dehydrogenase deficiency — (MCAD) Classification and external resources ICD 9 277.85 OMIM 201450 … Wikipedia
Newborn screening — See also: Apgar score Newborn screening Intervention MeSH D015997 Newborn screening is the process by which infants are screened shortly after birth for a list of disorders that are treatable, but di … Wikipedia
Rhabdomyolysis — Classification and external resources Urine from a person with rhabdomyolysis showing the characteristic brown discoloration as a result of myoglobinuria … Wikipedia
ДЕФЕКТЫ АЦИЛ-КОА ДЕГИДРОГЕНАЗ — мед. К ацил КоА дегидрогеназам, осуществляющим р окисление в митохондриях, отнесён ряд ферментов. Врождённые дефекты митохондриального р окисления недостаточность ацил КоА дегидрогеназ (все р): короткоцепочечной (201470, SCAD), среднецепочечной… … Справочник по болезням
