tay sachs dis eases

Tay-Sachs disease

[tey-saks]
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:
1920–25; named after W. Tay (1843–1927), English physician, and B. Sachs (1858–1944), American neurologist

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Collins
World English Dictionary
Tay-Sachs disease (ˌteɪˈsæks)
 
n
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
 
[C20: named after W. Tay (1843--1927), British physician, and B. Sachs (1858--1944), US neurologist]

Collins English Dictionary - Complete & Unabridged 10th Edition
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American Heritage
Medical Dictionary

Tay-Sachs disease (tā'sāks')
n.
A lyposomal storage disease that is the infantile type of cerebral sphingolipidosis. Also called GM2 gangliosidosis.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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American Heritage
Science Dictionary
Tay-Sachs disease   (tā'sāks')  Pronunciation Key 
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).
The American Heritage® Science Dictionary
Copyright © 2002. Published by Houghton Mifflin. All rights reserved.
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