MCAD deficiency

MCAD deficiency
MCAD de·fi·cien·cy medium-chain acyl-CoA dehydrogenase deficiency; see under acyl-CoA dehydrogenase.

Medical dictionary. 2011.

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  • 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

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