| Tay-Sachs disease |
Tay-Sachs disease is a rare inherited disorder that causes progressive destruction of nerve cells in the brain and spinal cord. The most common form of Tay-Sachs disease begins in infancy. An infant with the disorder appears normal until the age of 3 to 6 months, when development slows and the baby is often unable to crawl, turn over, or grasp objects. As the disease progresses, infants develop seizures, vision and hearing loss, mental retardation, and paralysis. ...
출처: goldbamboo.com/glossary-1t.html
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| Tay-Sachs disease |
Hereditary disorder resulting from a deficiency of the enzyme hexosaminidase. Symptoms include blindness, delayed development, seizures and paralysis. Tay-Sachs disease often results in an early death.
출처: www.allaboutvision.com/resources/glossary-3.htm
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| Tay-Sachs disease |
A genetic disorder carried by an estimated one in 30 Eastern European Jews; babies born with Tay-Sachs lack an essential enzyme and die in early childhood. A preconception test can determine whether potential parents are carriers of the disease.
출처: www.babycenter.com/glossary/T
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| Tay-Sachs disease |
Progressive nervous system disorder characterized by deafness, blindness, and seizures. The disease is fatal, usually by the age of 4.
출처: www.sparkle.usu.edu/glossary/syndromes_glossary.as...
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| Tay-Sachs disease |
Inherited disease characterized by mental and physical retardation, convulsions, enlargement of the head and eventually death. Trait is usually carried by Ashkenazi Jews.
출처: www.pregnancy-info.net/newprgnancyarticle13-5.html
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