Tay-Sachs disease - Wikipedia, the free encyclopedia
|
|
Tay-Sachs disease (abbreviated TSD , also known as GM2 gangliosidosis or Hexosaminidase A deficiency ) is an autosomal recessive genetic disorder. In its most common variant known as infantile ...
en.wikipedia.org/wiki/Tay-Sachs_disease
|
|
National Tay-Sachs and Allied Diseases Association of Delaware Valley (NTSAD-DV) is a non-profit, volunteer health agency dedicated to the prevention and elimination of Tay-Sachs, Canavan and the allied diseases. ... Tay-Sachs and Canavan diseases can be prevented. Anyone can be a carrier. Find out your risk of having a...
|
|
www.tay-sachs.org/
www.tay-sachs.org/
· Cached
|
|
|
|
What is Tay-Sachs Disease? ... Infants with Tay-Sachs disease appear to develop normally for the first few months of life. Then, as nerve cells become distended with fatty material, a relentless deterioration of mental and physical abilities occurs.
|
|
www.ninds.nih.gov/disorders/taysachs/taysachs.htm
www.ninds.nih.gov/disorders/taysachs/taysachs.htm
· Cached
|
|
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 mental development. ... Who Is at Risk for Tay-Sachs?
|
|
kidshealth.org/parent/medical/genetic/tay_sachs.html
kidshealth.org/parent/medical/genetic/tay_sachs.html
· Cached
|
|
The mission of the National-Tay Sachs & Allied Diseases Association is to lead the fight to treat and cure Tay-Sachs, Canavan and related genetic diseases and to support affected families and individuals in leading fuller lives.
|
The most common form of Tay-Sachs disease becomes apparent in infancy. Infants with this disorder typically appear normal until the age of 3 to 6 months, when their development slows and muscles used for movement weaken.
|
|
ghr.nlm.nih.gov/condition=taysachsdisease
ghr.nlm.nih.gov/condition=taysachsdisease
· Cached
|
|
Your Genes, Your Health, DNA Learning Center's multimedia guide to genetic, inherited disorders: Tay-Sachs disease, autosomal recessive, genetic disorder ... Tay-Sachs disorder. At-risk parents are encouraged to be tested before pregnancy to prepare for the possibilities. This kind of carrier screening...
25k - 4 sec @ 56k
This site uses Flash
|
www.ygyh.org/tay/whatisit.htm
www.ygyh.org/tay/whatisit.htm
· Cached
|
|
Tay-Sachs disease occurs when the body lacks hexosaminidase A, a protein that helps break down a chemical found in nerve tissue called gangliosides. Without this protein, gangliosides, particularly ganglioside GM2, build up in cells, especially nerve cells in the brain.
|
|
www.nlm.nih.gov/medlineplus/ency/article/001417.htm
· Cached
|
|