Examples of 'tay-sachs' in a sentence
Meaning of "tay-sachs"
Tay-Sachs: a genetic disorder that results in the destruction of nerve cells in the brain and spinal cord, typically leading to death in early childhood
How to use "tay-sachs" in a sentence
Basic
Advanced
tay-sachs
Have a confirmed diagnosis of Tay-Sachs disease.
The treatment of Tay-Sachs disease is supportive in nature.
Presently there is no treatment for Tay-Sachs.
Carriers of Tay-Sachs disease also show incomplete dominance.
Sarah was not showing any symptoms of Tay-Sachs.
A child suffering with Tay-Sachs disease looks healthy at birth.
An example of an autosomal recessive disorder is Tay-Sachs disease.
The most common form of Tay-Sachs disease becomes apparent in infancy.
Are at increased risk for the Tay-Sachs gene.
Babies born with Tay-Sachs rarely live beyond the age of four.
These alleles are associated with Tay-Sachs disease.
Infants with Tay-Sachs disease appear to develop normally for the first six months after birth.
These symptoms are similar to those of Tay-Sachs disease.
Tay-Sachs patients are missing a key enzyme.
This fatal genetic disorder is called Tay-Sachs disease.
See also
Tay-Sachs disease is an example of a recessive disorder.
Beutler made major contributions to the understanding of Tay-Sachs disease.
Tay-Sachs disease is an inherited disease caused by an abnormal gene.
The classic infantile type of Tay-Sachs is the most common.
And then they found out that he was a carrier for tay-sachs.
A ganglioside is a form of sphingolipid, which makes Tay-Sachs disease a member of the sphingolipidoses.
Absence of enzymes from this organelle can lead to storage diseases such as Tay-Sachs disease.
We can extend the life of children born with Tay-Sachs or other terminal genetic diseases.
Because they thought there was no chance they could have a Tay-Sachs baby.
Tay-Sachs disease is a fatal disease affecting the central nervous system.
Tay syndrome should not be confused with the Tay-Sachs disease.
Tay-Sachs can occur when parents pass on a changed gene to their child.
This is the cause of the signs and symptoms of Tay-Sachs disease.
Cystic fibrosis, Tay-Sachs disease and hemoglobinopathies are examples of relatively common Mendelian conditions.
Genetic screening has drastically reduced the number of Tay-Sachs babies.
Tay-Sachs Disease is a fatal disorder that causes a progressive degeneration of the central nervous system.
Frameshift mutations may result in severe genetic diseases such as Tay-Sachs disease.
Tay-Sachs Disease is an example of incomplete dominance in humans.
So there is very little chance that you carry the Tay-Sachs gene.
Tay-Sachs disease is an inherited disorder.
A child who inherits the anomalous gene from both the parents develops Tay-Sachs disease.
Programs have been able to nearly eliminate Tay-Sachs disease from the Jewish population.
Certainly not for individuals who inherited two copies of the mutation and had Tay-Sachs.
The first recorded case of Tay-sachs disease was.
Both Tay-Sachs disease and Sandhoff disease.
It has a similar pathology to Sandhoff disease and Tay-Sachs disease.
Tay-Sachs disease is a hereditary disorder.
French Canadians face an increased risk of Tay-Sachs and cystic fibrosis.
Tay-Sachs Disease is an autosomal recessive resulting in degeneration of the nervous system.
Genetic defects in the HEXA gene are responsible for Tay-Sachs lysosomal disease.
Tay-Sachs is most common among certain ethnic groups, particularly the Jewish community.
Part of the evidence is that no Semitic people ever suffer from Tay-Sachs disease!
Tay-Sachs disease is a serious genetic disorder common in Ashkenazi Jews and French-Canadians.
The goal is to diagnose genetic abnormalities, such as Down syndrome and Tay-Sachs disease.
Every Jewish couple I know got tested for Tay-Sachs before they walked down the aisle.
