If you have a history with the disease it is verry likely you may bing back to it.
Tay-Sachs disease is abbreviated to TSD and is also known as GM2 gangliosidosis or Hexosaminidase A deficiency.
The DNA sequence of the allele that causes Tay-Sachs disease is different from that of the normal allele. This difference in the DNA sequence allows for specific genetic tests to be conducted to identify the presence of the Tay-Sachs disease allele in individuals.
In Pompe's disease, the defect lies in the lysosomal enzyme alpha-glucosidase, which leads to the accumulation of glycogen in lysosomes. In Tay-Sachs disease, the defect is in the enzyme hexosaminidase A, which leads to the accumulation of GM2 gangliosides in lysosomes.
The gene that causes Tay-Sachs disease normally provides instructions for making an enzyme called hexosaminidase A. This enzyme helps break down a fatty substance called GM2 ganglioside. Mutations in this gene lead to a deficiency in hexosaminidase A, causing the buildup of GM2 ganglioside in cells, which leads to the symptoms of Tay-Sachs disease.
The part of tay sachs that kills you is recessive. Some proteins are still expressed even if you are a heterzygous carrier of tay sachs (less than if you are homozygous recessive but more than homozygous dominant) making the molecular view of tay sachs codominant.
what effect does Tay-sachs disease have on the body?
Tay-Sachs disease is a human genetic disorder.
what effect does Tay-sachs disease have on the body?
A person with tay sachs can live a healthy life but still battles the many limitations of Tay sachs disease. Depending on the type of tay sachs, Classic, Juvenile onset, and Late Onset depends how healthy a life a person with tay sachs disease.
About 16 cases of Tay-Sachs disease are diagnosed each year.
Tay-Sachs disease is abbreviated to TSD and is also known as GM2 gangliosidosis or Hexosaminidase A deficiency.
Although there are extremely rare cases of adult onset Tay Sachs disease, it generally strikes very young children, killing them before they are pre-teens, There are not any celebrities who have spoken about having Tay Sachs disease.
There is no evidence that shows that tay-sachs is a sex-linked trait.
There is no evidence that shows that tay-sachs is a sex-linked trait.
''Tay-Sachs'' was named after Warren Tay, an ophthalmologist who discovered the occurring red spot in the retina in 1881, and Bernard Sachs, who described the cellular changes related to this disease in 1887.
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).
Tay-sachs disease differs from an infectious disease because it is a hereditary disease, so it can only be passed from parents to their offspring.