mcardle disease
1McArdle 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.) …
2McArdle disease (syndrome) — Mc·Ar·dle disease (syndrome) (mək ahrґdəl) [Brian McArdle, English neurologist, 1911–2002] see glycogen storage disease, type V, under disease …
3McArdle disease — glycogen storage d., type V …
4McArdle-Krankheit — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit …
5McArdle-Syndrom — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit …
6McArdle — Irish name:MacArdghail Ethnicity Irish/Celtic Information Place of origin County Monaghan, Ireland[1] Notable members …
7McArdle'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 …
8McArdle's disease — ▪ pathology also called Glycogenosis Type V, rare hereditary deficiency of the enzyme glycogen phosphorylase in muscle cells. In the absence of this enzyme, muscles cannot break down animal starch (glycogen) to meet the energy… …
9Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… …
10McArdle'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,… …