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Tay-Sachs disease!!!!!!!? |
Do people with Tay-Sachs disease look different than normal people? I need a quick answer! THXXX! They have a cherry red spot on them, see the Wikipedia page below for a complete description. There was a special on discovery health. The girl did look quite different but not sure if they all do. She needed alot of surgery. Maybe you can google images of it. Thats what I did when the baby I carried had Trisomy 13. well the majority of people with Tay Sachs are Jewish babies. And I think that you can't see it until it really hits, then it's obvious, with discoloration and stuff. Infantile TSD. Infants with Tay-Sachs disease appear to develop normally for the first six months of life. Then, as nerve cells become distended with gangliosides, a relentless deterioration of mental and physical abilities occurs. The child becomes blind, deaf, and unable to swallow. Muscles begin to atrophy and paralysis sets in. Death usually occurs before the age of 3. |
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I think it's recessive alleles. Both parents must be a carrier. Infants with Tay-Sachs disease appear to develop normally for the first six months of life. Then, as nerve cells become disten... TSD is a recessive genetic disorder, meaning that both parents must be carriers in order to give birth to an affected child. Even then, there is only a 25% chance with each pregnancy of having a ch... Rare in the UK (can't find any numbers!) - 1 in 360,000 live births worldwide, so probably less than 1000 each year. ...Tay-Sachs disease occurs when the body lacks hexosaminidase A, a protein that helps break down a chemical found in nerve tissue called gangliosides. Without this protein, gangliosides, particularly... They are categorized as autosomal recessive diseases, because the parents must possess these traits in their recessives in order to pass it along to their offspring. ...for children over the age of 6mos. Extremely Rare. it is also rare to extremely rare for adults to get TSD also. The most common form is infantile TSD and is usually diagnosed by 7mos. old. 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. The condition i... Genetic diseases are passed within that culture....only plenty out breeding out of that culture will change the genetic bloodlines that dominate the disease. Sickle cell stricks only African Ameri... |
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