glycogenosis

[gli″ko-jĕ-no´sis] glycogen storage disease.generalized glycogenosis Pompe's disease.hepatorenal glycogenosis Gierke's disease.myophosphorylase deficiency glycogenosis McArdle disease.

gly·co·ge·no·sis

(glī'kō-jĕ-nō'sis), Any of the glycogen deposition diseases characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the tongue, with progressive muscular weakness. Seven types (Cori classification) are recognized, depending on the enzyme deficiency involved, all of autosomal recessive inheritance, but with a different gene for each enzyme deficiency. [MIM designations: I, *232200, *232220, *232240; II, *232300; III, *232400; IV, *232500; V, *232600; VI, *232700; VII, *232800]. Synonym(s): dextrinosis, glycogen-storage disease

glycogenosis

(glī′kə-jĕ-nō′sĭs)n. pl. glycogeno·ses (-sēz′) See glycogen storage disease.

glycogenosis

Glycogen storage disease, see there.

gly·co·ge·no·sis

(glī'kō-jĕ-nō'sis) Any glycogen deposition disease characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the tongue, with progressive muscular weakness.
Synonym(s): dextrinosis.

Glycogenosis

An alternate term for glycogen storage disease. The plural form is glycogenoses.Mentioned in: Glycogen Storage Diseases

gly·co·ge·no·sis

(glī'kō-jĕ-nō'sis) A glycogen deposition disease characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; may be enlargement of the liver, heart, or striated muscle, including the tongue.

单词	glycogenosis
释义	glycogenosis gly·co·ge·no·sis G5169950 (glī′kə-jĕ-nō′sĭs)n. pl. gly·co·ge·no·ses (-sēz′) See glycogen storage disease. glycogenosis glycogenosis [′glī·kō·jə′nō·səs] (medicine) One of several inborn errors in the metabolism of glycogen, classified on the basis of the enzyme deficiency and clinical findings as von Gierke's disease, Pompe's disease, limit dextrinosis, amylopectinosis, McArdle's disease, or Hers' disease. glycogenosis glycogenosis [gli″ko-jĕ-no´sis] glycogen storage disease.generalized glycogenosis Pompe's disease.hepatorenal glycogenosis Gierke's disease.myophosphorylase deficiency glycogenosis McArdle disease. gly·co·ge·no·sis (glī'kō-jĕ-nō'sis), Any of the glycogen deposition diseases characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the tongue, with progressive muscular weakness. Seven types (Cori classification) are recognized, depending on the enzyme deficiency involved, all of autosomal recessive inheritance, but with a different gene for each enzyme deficiency. [MIM designations: I, 232200, 232220, 232240; II, 232300; III, 232400; IV, 232500; V, 232600; VI, 232700; VII, 232800]. Synonym(s): dextrinosis, glycogen-storage disease glycogenosis (glī′kə-jĕ-nō′sĭs)n. pl.* glycogeno·ses (-sēz′) See glycogen storage disease. glycogenosis Glycogen storage disease, see there. gly·co·ge·no·sis (glī'kō-jĕ-nō'sis) Any glycogen deposition disease characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the tongue, with progressive muscular weakness. Synonym(s): dextrinosis. Glycogenosis An alternate term for glycogen storage disease. The plural form is glycogenoses.Mentioned in: Glycogen Storage Diseases gly·co·ge·no·sis (glī'kō-jĕ-nō'sis) A glycogen deposition disease characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; may be enlargement of the liver, heart, or striated muscle, including the tongue.
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