Tay-Sachs disease is a rare hereditary disorder that occurs when the body lacks an enzyme that can break down fatty ...

In one particular variant of this disease known as mucopolysaccharidosis I (MPS I), a deficiency of the enzyme alpha-L-iduronidase causes a build up of GAGs in tissues and organs, which in turn ...

Carrying Tay-Sachs disease may protect against tuberculosis (TB). In Ashkenazim populations, up to 11 percent of the people are Tay-Sachs carriers. During World War II, TB ran rampant in Eastern ...

Accumulation of fat molecules is detrimental to the cell. Researchers from the Yong Loo Lin School of Medicine, National ...

Scientists from Brigham and Women’s Hospital have now identified a new protein that may contribute to the disease.

Jewish Genetic Screening Awareness Week is very important in educating the public and advocating for widespread screening.

Dr. Matt Goldstein and Myra Sack lost their daughter, Havi, to Tay-Sachs disease in 2021. Tay-Sachs is a rare, inherited genetic disease primarily affecting infants and young children. There is no ...

The heroes are voluntary organizations like the Wellcome Trust or the Committee for the Prevention of Jewish Genetic Disease, which has done much to eliminate Tay-Sachs disease and cystic fibrosis ...

Fabry disease and GM2 gangliosidosis (also known as Tay-Sachs disease), but the company's earlier assessment of venglustat as a "pipeline in a pill" is starting to look shaky. The phase 2/3 STAGED ...