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Published byPearl James Modified over 9 years ago
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By: Aaron Nachtigall and Ethan Adcock
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Tay-Sachs was named after Warren Tay, because in 1881 he described a patient with a cherry-red spot on the retina of the eye. It is also named Tay-Sachs because a few years later Bernard Sachs discovered that Tay-Sachs is a cellular defect. It was first commonly seen in Eastern European Jews.
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This disease occurs when there is a lack of a protein that breaks down a chemical found in nerve tissue. It is cause by a defective gene on chromosome 15. This disease is recessive, both parents must pass the gene to their child.
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Deafness Blindness Loss of muscle strength Delayed mental and social skills Dementia Loss of muscle function Seizures Slow growth Death
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1 in 250 people carry the gene In the Ashkenazi Jewish population however 1 in 27 members carry the gene.
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Children with a lot of care are still projected to die at the age of 5. The first test tube baby ever born was born with the Tay Sachs disease. The first symptoms of the disease occur when the baby is 6 months old, when the lose the ability to smile.
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A.D.A.M Medical Encylapedia. “Tay-Sachs Disease.” 17 November 2010. Web. 2012 “History of Tay-Sachs Disease.” National Tay-Sachs and Allied Diseases. Web. 2012 “Tay-Sachs disease.” October 2012. Web. 2012
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