The disease is named after the British ophthalmologist Warren Tay who first described the red spot on the retina of the eye in 1881, and the American neurologist Bernard Sachs of Mount Sinai Hospital, New York who described the cellular changes of Tay-Sachs and noted an increased prevalence in the Eastern European Jewish (Ashkenazi) population in 1887.It was named because thay practily discovered it
if someone is a Heterozygous carrier of Tay-Sachs they would have to be Tt. Because TT is Homozygous.
its inherited from family member to family member
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 is a human genetic disorder which results in the accumulation of cells due to the clogging caused by undigested lipids. The organelle involved in this disease is the lysosome.
No; it is a genetic mutation that is passed from parent to child so therefore it is a problem in the genes and cannot be cured.
It was named after doctors Warren Tay and Bernard Sachs.
''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.
Tay-Sachs was named after Wamen Tay and Bernard Sachs Correction: Tay-Sachs was named after Warren Tay and Bernard Sachs
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!! Discovered in 1881.
They were the two people directly responsible for identifying Tay Sachs Disease or aka TSD. It was first identified by British ophthalmologist Warren Tay in 1881 and American physician Bernard Sachs in 1887, consequently receiving its name "Tay-Sachs". Tay concentrated on eye changes and described eye defects in an infant with a progressive neurological disease. This is also known as a "cherry-red spot" found in the macula in the back of the eye, it's a characteristic of this disorder. Sachs focused on clinical features, diagnostic signs and pathology, he presented his observations of a disease that was common among German immigrants of Jewish heritage. TSD is most common in Ashkenazi Jews, which are Jews descending from Central or Eastern Europe, and it's also found in some French Canadians. This disease is an autosomal recessive condition meaning that a carrier isn't affected by it but if two carriers cross then there is a 25% chance of a child being affected by it.
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.
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!
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.
Sorry, Tay-Sachs is not a germ-caused infectious disease, so there is no incubation period, at all. Tay-Sachs is inherited from a person's mother and father.