- MCAD deficiency
- MCAD de·fi·cien·cy medium-chain acyl-CoA dehydrogenase deficiency; see under acyl-CoA dehydrogenase.
Medical dictionary. 2011.
Medical dictionary. 2011.
MCAD — may refer to: * Medium chain acyl dehydrogenase deficiency * Microsoft Certified Application Developer * Mechanical computer aided design * Minneapolis College of Art and Design * Modern and Classic Automobile Discussion … Wikipedia
medium-chain acyl-CoA dehydrogenase (MCAD) deficiency — a defect in mitochondrial beta oxidation due to a mutation in the gene (locus: 1p31) encoding acyl CoA dehydrogenase that acts on medium chain length fatty acids. It is characterized by recurring episodes of hypoglycemia, vomiting, and lethargy,… … Medical dictionary
deficiency — An insufficient quantity of some substance (as in dietary d. or hemoglobin d. in marrow aplasia); organization (as in mental d.); activity (as in enzyme d. or reduced oxygen carrying capacity of the blood), etc., of which the amount present is of … Medical dictionary
MCAD — abbr. and/or acronym. Medium chain acyl CoA dehydrogenase deficiency … American Life League. Abbreviations and acronyms
Medium-chain acyl-coenzyme A dehydrogenase deficiency — (MCAD) Classification and external resources ICD 9 277.85 OMIM 201450 … Wikipedia
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
Sudden infant death syndrome — Classification and external resources ICD 10 R95 ICD 9 798.0 … 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
Medium-Chain-Acyl-CoA-Dehydrogenase-Mangel — Klassifikation nach ICD 10 E71.3 Störungen des Fettsäurestoffwechsels … Deutsch Wikipedia
metabolic disease — ▪ pathology Introduction any of the diseases or disorders that disrupt normal metabolism, the process of converting food to energy on a cellular (cell) level. Thousands of enzymes participating in numerous interdependent metabolic pathways… … Universalium