| 释义 |
lipid storage disease
lipid storage disease[′lip·əd ‚stȯr·ij di‚zēz] (medicine) Any of various rare diseases characterized by the accumulation of large histiocytes containing lipids throughout reticuloendothelial tissues; examples are Goucher's disease, Niemann-Pick disease, and amaurotic familial idiocy. lipid storage disease
lipid storage diseaseA group of rare inherited disorders of fat metabolism in which lipids are metabolized abnormally and accumulate in tissues such as the brain and peripheral nerves. |