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Tay-Sachs disease
[ tey-saks ]
noun
- 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
- 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
Tay-Sachs disease
/ tā′săks′ /
- 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).
Word History and Origins
Origin of Tay-Sachs disease1
Word History and Origins
Origin of Tay-Sachs disease1
Example Sentences
Tay-Sachs disease, the more common of the two disorders, typically manifests within the first year of life, progressing quickly and often proving fatal within a few years.
A child with Tay-Sachs disease can appear radiantly healthy as a newborn but begins an inexorable decline by six months.
Disabled by late-onset Tay-Sachs disease, a neurological condition, she had been hospitalized with an uncertain prognosis.
Two babies have received the first-ever gene therapy for Tay-Sachs disease after over 14 years of development.
In her third memoir, Emily Rapp Black writes of tentatively, painfully regaining her footing after losing her son to Tay-Sachs disease.
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