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Tay-Sachs disease

[ tey-saks ]

noun

, Pathology.
  1. a rare fatal hereditary disease, occurring chiefly in infants and children, especially of eastern European Jewish origin, characterized by a red spot on the retina, gradual blindness, and paralysis.


Tay-Sachs disease

/ ˌteɪˈsæks /

noun

  1. an inherited disorder, caused by a faulty recessive gene, in which lipids accumulate in the brain, leading to mental retardation and blindness. It occurs mostly in Ashkenazi Jews
“Collins English Dictionary — Complete & Unabridged” 2012 Digital Edition © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins Publishers 1998, 2000, 2003, 2005, 2006, 2007, 2009, 2012


Tay-Sachs disease

/ săks′ /

  1. A genetic disease in which the products of fat metabolism accumulate in the nervous system, causing retardation, paralysis, and death by preschool age. Individuals of eastern European Jewish descent have a higher risk of inheriting Tay-Sachs disease. The disease is named after its describers, British ophthalmologist Warren Tay (1843–1927) and American neurologist Bernard Sachs (1858–1944).


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Word History and Origins

Origin of Tay-Sachs disease1

1920–25; named after W. Tay (1843–1927), English physician, and B. Sachs (1858–1944), American neurologist
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Word History and Origins

Origin of Tay-Sachs disease1

C20: named after W. Tay (1843–1927), British physician, and B. Sachs (1858–1944), US neurologist

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