Results 1 - 6 of 6 for Tay Sachs disease
  1. Tay-Sachs disease is a rare inherited disorder that progressively destroys nerve cells (neurons) in the brain and spinal cord.The most common form of Tay-Sachs disease becomes apparent in infancy. Infants with this disorder ...
  2. ... GM2 ganglioside. More than 120 mutations that cause Tay-Sachs disease have been identified in the HEXA gene. These ... cells, which causes the signs and symptoms of Tay-Sachs disease.Most of the known HEXA mutations result in ...
  3. ... AB variant Activator Deficiency/GM2 Gangliosidosis Activator-deficient Tay-Sachs disease GM2 Activator Deficiency Disease GM2 gangliosidosis, type AB ...
  4. ... B: understanding the molecular basis of Sandhoff and Tay-Sachs disease. J Mol Biol. 2003 Apr 11;327(5): ... Y, Tifft CJ, Proia RL. Molecular pathophysiology in Tay-Sachs and Sandhoff diseases as revealed by gene expression profiling. Hum Mol ...
  5. ... also called sickle cell anemia Sjögren-Larsson syndrome Tay-Sachs disease Tyrosinemia Usher syndrome Zellweger spectrum disorder , also called ...
  6. ... of African, African American, or Mediterranean heritage; and Tay-Sachs disease , which is more likely to occur among people ...