There are a couple ways Tay-Sachs can be prevented;
1) determine if both you and your mate carry the Tay-Sachs gene
2) perform a prenatal diagnosis to determine if the fetus carries the Tay-Sachs gene
Hope this helped!
No...no way. kolkata sucks
. One potential treatment focuses on the lack of the hexosaminidase A enzyme. If the enzyme can be replaced, then the GM2 deposits could be broken down into their component parts, and nerve cells could return to a state of proper function.
The cast of Which Way Is East - 1994 includes: Dana Sachs as herself Lynne Sachs as herself
It is unknown how many people have Tay-Sachs disease because sometimes the illness is misdiagnosed or not diagnosed in patients. However, it is a very rare disorder that is more common for people with an eastern and central European background.
no
NO
it falled down in 2000
Carmex
There are three forms of Tay-Sachs disease, categorized by the types of symptoms and the age when the symptoms first appear. The most common form appears when the child is 3 to 6 months old, with the disease progressing rapidly to death by age 4 or 5. At birth, the infant appears healthy and develops normally for the first few months of life, but as the buildup of ganglioside GM2 begins to affect nerves, symptoms appear. Initially, symptoms may include: * Seizures * Noticeable behavior changes, such as the infant stops smiling, crawling or rolling over and loses the ability to grasp or reach out * Increased startle reaction * Decreased eye contact * Listlessness * Increasing irritability * Slow body growth with increasing head size * Delayed mental and social skills As the disease progresses, these symptoms become more dominant: * Feeding difficulties * Abnormal body tone * Loss of motor skills * Blindness * Deafness * Loss of intellectual skills Much rarer are the forms of Tay-Sachs that develop later in life and are due to low levels of the hex A enzyme, rather than the complete deficiency of hex A in the infantile form. Children with juvenile hex A deficiency develop symptoms between ages 2 and 5, and usually die by age 15. A milder form of hex A deficiency can develop anywhere from age 5 to the early 30s. Symptoms include slurred speech, an unsteady gait, tremors and, sometimes, mental illness.
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The laws of nature conspire to prevent it from being any other way.
because that's the way God made him