Answer: Tay-Sachs disease is a hereditary illness. The body does not make a molecule that is required to break down fatty substances in the body, called gangliosides. The gangliosides collect in the nervous tissue, resulting in damage to the brain and nerves.
Answer: A mutation of the HEX A gene of chromosome 15 causes Tay-Sachs disease. As a result, the protein hexosaminidase A is not formed properly and GM2 ganglioside, the lipid normally broken down by hexosaminidase A, accumulates to toxic levels (especially in the brain).
Answer: First you take a physical exam and a blood test that tests the level of hex-A, the protein this disease affects, in your body. If the first blood test comes out positive, there may be other additional genetic tests to see for sure whether or not you have Tay Sachs.
Answer: until complete heart failure and biological death!
addition: Tay-Sachs disease is a fatal genetic lipid storage disorder in which harmful quantities of a fatty substance called ganglioside GM2 build up in tissues and nerve cells in the brain. Presently there is no treatment for Tay-Sachs disease. Anticonvulsant medicine may initially control seizures. Other supportive treatment includes proper nutrition and hydration and techniques to keep the airway open. Children may eventually need a feeding tube. Even with the best of care, children with Tay-Sachs disease usually die by age 4, from recurring infection. At the present time, the prognosis for a baby born with Tay-Sachs disease is certain death. Nothing can be done to keep the baby alive.
Answer: Depend on the age of onset but anywhere from death, loss of sight, loss of hearing, paralysis..etc in babies to cognitive, motor, swallowing, and speech difficulties to even psychosis in adults.
Answer: In Tay-Sachs disease, a mutation that affects the alpha subunit of the enzyme causes a deficiency in HexA. Sandhoff disease is caused by mutations that affect the beta subunit, rendering both the HexA and HexB enzymes deficient.
Answer: Sadly, the prognosis for a child with classic Tay-Sachs disease is certain death. Because the chronic form of Tay-Sachs has been discovered recently, prognosis for this type of the disease is not completely known.
What effect does Tay-Sachs disease have on the body?
what effect does Tay-sachs disease have on the body?
Answer: Some known treatments for Tay-Sachs disease are: · Medication · Techniques to keep airways opened And · Proper nutrition/hydration These are some treatments that are said to help treat Tay-sachs disease. But, there is no known treatment that will for sure cure it.
Answer: Symptoms of Tay-Sachs disease were discovered by Warren Tay in 1881 and Bernard Sachs wrote about it in general in 1887. (this is a disease which affects the brain and eventually kills the person who has it.) Infants that have Tay-Sachs normally die by age 5. They start to lose their functions by the age of 8 months!!