McArdle's disease — McArdle s disease, McBurney s point see entries alphabetized as MC Mc·Ar·dle s disease mək ärd əlz n glycogen storage disease that is inherited as an autosomal recessive trait, is marked esp. by muscle weakness and myoglobinuria, and is caused by … Medical dictionary
McArdle's disease — noun an inherited disease in which abnormal amounts of glycogen accumulate in skeletal muscle; results in weakness and cramping • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease,… … Useful english dictionary
McArdle's disease — an inborn error of metabolism in which a deficiency of the enzyme myophosphorylase prevents the breakdown of glycogen to lactate in exercising muscle. This results in fatigue, pain, and cramps in exercising muscles. The only treatment is… … The new mediacal dictionary
McArdle's disease — Glycogen storage disease in which the defective enzyme is muscle phosphorylase … Dictionary of molecular biology
McArdle's disease — noun Glycogen storage disease type V, a metabolic disorder caused by a deficiency of myophosphorylase … Wiktionary
McArdle — Irish name:MacArdghail Ethnicity Irish/Celtic Information Place of origin County Monaghan, Ireland[1] Notable members … Wikipedia
McArdle-Krankheit — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit … Deutsch Wikipedia
McArdle-Syndrom — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit … Deutsch Wikipedia
McArdle disease — McArdle disease. См. гликогеноз V типа. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
McArdle disease (syndrome) — Mc·Ar·dle disease (syndrome) (mək ahrґdəl) [Brian McArdle, English neurologist, 1911–2002] see glycogen storage disease, type V, under disease … Medical dictionary