dextrinosis

[dek″strĭ-no´sis] a condition characterized by accumulation in the tissues of an abnormal polysaccharide.limit dextrinosis Forbes' 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

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.

单词	dextrinosis
释义	DictionarySeeglycogenosisEncyclopediaSeeglycogen storage disease dextrinosis dextrinosis [dek″strĭ-no´sis] a condition characterized by accumulation in the tissues of an abnormal polysaccharide.limit dextrinosis Forbes' 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 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.
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