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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 Disease
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. More »
Source: healthline.com

TaySachs disease


TaySachs disease (also known as GM2 gangliosidosis or hexosaminidase A deficiency) is a rare autosomal recessive genetic disorder. In its most common ...

Tay-Sachs disease - Genetics Home Reference


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-Sachs disease. Find out why people of Jewish decent are most at risk of having children with Tay-Sachs. More »

Tay-Sachs Disease - National Library of Medicine - PubMed Health


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 ...

Learning About Tay-Sachs Disease


Answers to frequently asked questions about Tay-Sachs disease, published by the National Human Genome Research Institute.

Tay-Sachs Disease - KidsHealth


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 ...

Tay-sachs Disease :: National Tay-Sachs & Allied Diseases ...


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 of ...

Tay-Sachs Disease - Center for Jewish Genetics


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 ...

Tay Sachs Disease Symptoms
Tay Sachs Disease is a genetic defect that prevents the body from producing the necessary level of the enzyme hexosaminidase A. This enzyme is responsible for the breakdown of GM2 gangliosides (a fatty substance). This results in a build-up of GM2... More »
Difficulty: Easy
Source: www.ehow.com
Popular Q&A
Q: What is is tay sachs disease?
A: It is a mental retardation when both parents have the same genes that create it. most children die before they are 6. ya what they said hey jimmy!!!!!!! Read More »
Source: wiki.answers.com
Q: What is Tay Sachs disease?
A: tay - sachs disease is when you are born without hexosinidase.... it messes up your nerves and changes your physical appearance after a few months Read More »
Source: wiki.answers.com
Q: What is the tay sachs disease?
A: Tay-Sachs disease is a rare genetic disorder in which little or no hexosaminidase A Read More »
Source: www.chacha.com
Q: What is Tay Sachs disease
A: Tay-Sachs disease is a fatal genetic lipid storage disorder in whic... ...MORE... Read More »
Source: www.chacha.com
Q: What is tay sachs disease?
A: found this article helpful. Topic Overview What is Tay-Sachs disease? Tay-Sachs disease is a rare genetic disorder in which little or no hexosaminidase A (hex A... Read More »
Source: answers.yahoo.com