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单词 Tay-Sachs disease
释义

Tay-Sachs disease/ˌtay ʹsaks/ noun

a rare hereditary metabolic disorder involving an enzyme deficiency that causes a build-up of lipids (fatty substances; see lipid) in brain and nerve tissue, resulting in mental retardation, paralysis, epileptic seizures, blindness, and, ultimately, death. Tay-Sachs disease mostly affects very young children, esp of eastern European Jewish descent

[named after Warren Tay d.1927, British physician, and Bernard Sachs d.1944, American neurologist, who each independently described it]
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更新时间:2025/1/5 23:31:56