According to WebMD, Tay Sachs disease is an autosomal recessive disease, meaning both parents need to have a copy of the mutated gene in order to pass it onto their offspring. Tay ...
Tay-Sachs is a disease of the central nervous system; it is a neurodegenerative disorder. Tay-Sachs most commonly affects infants. In infants, it is a progressive disease that is unfortunately always fatal. Rarely, Tay-Sachs can occur in teens and adults, causing less severe symptoms.
Tay–Sachs disease (also known as GM2 gangliosidosis or hexosaminidase A
deficiency) is a rare autosomal recessive genetic disorder. In its most common ...
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 ...
Information about the causes, symptoms, diagnosis, and treatment of Tay
. Find out why people of Jewish decent are most at risk of having children with Tay
. More »
Tay-Sachs diseases causes a progressive deterioration of nerve cells and of
mental and physical abilities that begins around six months of age. The disease ...
Answers to frequently asked questions about Tay-Sachs disease, published by
the National Human Genome Research Institute.
A baby with Tay-Sachs disease is born without an important enzyme, so fatty
proteins build up in the brain, hurting the baby's sight, hearing, movement, and ...
A baby with Tay-Sachs disease appears healthy at birth, and seems to be
developing normally for a few months. Symptoms generally appear by six months
Tay-Sachs disease is the most familiar of the Jewish genetic disorders. It is
caused by a deficiency of an enzyme called hexosaminidase A, or hex A. This ...