Tay-Sachs disease

[ tey-saks ]
/ ˈteɪˈsæks /

noun Pathology.

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.

Origin of Tay-Sachs disease

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

British Dictionary definitions for tay-sachs disease

Tay-Sachs disease
/ (ˌteɪˈsæks) /

noun

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

Word Origin for Tay-Sachs disease

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

Medical definitions for tay-sachs disease

Tay-Sachs disease
[ tāsăks′ ]

n.

A liposomal storage disease that is the infantile type of cerebral sphingolipidosis. GM2 gangliosidosis

Scientific definitions for tay-sachs disease

Tay-Sachs disease
[ tāsăks′ ]

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).