| Tay-Sachs disease |
A fatal heredity disorder characterized by mental retardation and paralysis. This condition is most common in offspring from Jewish couples of eastern European descent.
출처: www.havingbabies.com/news/42_146_2982.cfm
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| Tay-Sachs disease |
An inherited disease of infancy characterized by profound mental retardation and early death; it is caused by a recessive gene mutation.
출처: www.knowledgene.com/public/glossary_content.php3
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| Tay-Sachs disease |
Tay-Sachs affects not only the eye but also the brain, causing early death.
출처: www.visionrx.com/library/enc/enc_retina.asp
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| Tay-Sachs d. |
the most common ganglioside storage disease, occurring almost exclusively among northeast European Jews. TSD is a GM2 gangliosidosis specifically characterized by infantile onset (3–6 months), doll-like facies, cherry-red macular spot (90+ per cent of the infants), early blindness, hyperacusis, macrocephaly, seizures, and hypotonia; the children die between 2 and 5 years of age. See also Sandhoff's d. and see GM2 gangliosidosis, variant B, under gangliosidosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Tay-Sachs disease |
is caused by a deficiency of the a cell chemical called hexoaminidase A. A harmful substance then builds up in the brain causing deterioration in both mental and physical abilities. Death typically occurs by 5 years of age. A less common form affects adults rather than children.
출처: www.enh.org/healthandwellness/clinicalservices/gen...
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