Tay-Sachs disease is abbreviated to TSD and is also known as GM2 gangliosidosis or Hexosaminidase A deficiency.
tay-sachs disease
TSD means Tay-Sachs Disease.
Lysosomes
Tay-Sachs disease
If you have a history with the disease it is verry likely you may bing back to it.
Tay–Sachs disease is also known as GM2 gangliosidosis or hexosaminidase A deficiency. Other names are: B variant GM2 gangliosidosis, GM2 gangliosidosis, type 1, Hexosaminidase alpha-subunit deficiency (variant B), Sphingolipidosis, Tay-Sachs and TSD.
Tay-Sachs disease is a human genetic disorder.
what effect does Tay-sachs disease have on the body?
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
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.