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sphingolipidosis
sphingolipidosis[¦sfiŋ·gō‚lip·ə′dō·səs] (medicine) Any of a group of hereditary metabolic disorders characterized by excessive accumulations of certain glycolipids and phospholipids in various tissues of the body. sphingolipidosis
sphingolipidosis [sfing″go-lip″ĭ-do´sis] a general designation applied to diseases characterized by abnormal storage of sphingolipids, such as gaucher's disease, niemann-pick disease, hurler's syndrome, and tay-sachs disease; all are associated with mental retardation and premature death.sphin·go·lip·i·do·sis (sfing'gō-lip'i-dō'sis), Collective designation for various diseases characterized by abnormal sphingolipid metabolism (for example, gangliosidosis, Gaucher disease, Niemann-Pick disease). Synonym(s): sphingolipodystrophysphingolipidosis (sfĭng′gō-lĭp′ĭ-dō′sĭs)n. Any of various diseases, such as Gaucher disease or Niemann-Pick disease, caused by a deficiency of an enzyme that degrades sphingolipids.sphin·go·lip·i·do·sis , sphingolipodystrophy, pl. sphingolipidoses (sfinggō-lipi-dōsis, -ō-distrŏ-fē, -i-dōsēz) Collective designation for a variety of diseases characterized by abnormal sphingolipid metabolism, e.g., gangliosidosis, Gaucher disease, Niemann-Pick disease. sphin·go·lip·i·do·sis, pl. sphingo lipidoses , sphingolipodystro phy (sfinggō-lipi-dōsis, -i-dōsēz, -ō-distrŏ-fē) Collective designation for various diseases characterized by abnormal sphingolipid metabolism. |