| 释义 |
DictionarySeediseaseMcArdle disease
McArdle disease [mik-ar´d'l] glycogen storage disease" >glycogen storage disease (type V), a condition in which deficiency of muscle phosphorylase results in accumulation of glycogen in skeletal muscles, with muscle cramps and a depressed blood lactate level during exercise. Called also myophosphorylase deficiency glycogenosis.gly·co·ge·no·sis type 5 (glī'kō-jĕ-nō'sis tīp) Disorder due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle tissue.
Synonym(s): McArdle disease, McArdle-Schmid-Pearson disease. McArdle disease (mak-ard'il) [Brian McArdle, Brit. pediatrician, 1911–2002] A glycogen storage disease caused by deficient myophosphorylase B (a muscle phosphorylase.) Synonym: glycogen storage disease type V; muscle phosphorylase deficiencyMcArdle, Brian, English neurologist, d. 2002. McArdle disease - Synonym(s): McArdle syndromeMcArdle syndrome - glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym(s): Cori syndrome; McArdle disease; McArdle-Schmid-Pearson syndrome; type 5 glycogenosisMcArdle-Schmid-Pearson disease - Synonym(s): McArdle syndrome |