Tay-Sachs Disease Essay

Running Head: THE SCOURGE OF TAY-SACHS Trosacks Case Study Name of Student School Interdisciplinary Team The members will be a physician, a geneticist, an ethicist, a lawyer and a nurse. The physician, who is a pediatrician, makes the diagnosis of Tay Sachs. The geneticist, another specialist, provides more specific and applicable information on Tay-Sachs, such as causes and risks, prevention, diagnosis and treatment. These two specialists formulate a plan of care, which a nurse will implement

Tay-Sachs disease is a disorder in the central nervous system. It is a disorder that most commonly affects infants. It is a disease that is most commonly always fatal. Tay-Sachs can also occur in teens and adults, causing less not fatal symptoms, although this occurs rarely. This disease is caused because you are missing an enzyme in the body named Hexosaminidase. Without this enzyme a fatty element called Ganglioside builds up on lysosomes which then this overcrowds the cells causing this to damage

The method of reproductive decision-making discussed here is carrier screening for Tay-Sachs disease. Non-directive counseling refers to the test being offered without influence on the client’s ultimate course of action. The decision to be tested should be completely voluntary and the sole choice of the individual. For example, if a clinician finds that a couple is both carriers for Tay-Sachs disease that clinician cannot then tell the couple that they must refrain from having children. A benefit

In Tay-Sach’s, the body does not have a particular enzyme that rids fatty tissues in the brain, allowing the fat build-up to persist (Specter). This causes the brain to slowly deteriorate as the baby matures, which annihilates the child by five years of age

Tay Sachs Disease is one of the most deadly and rarest disease known. This disease is shown in adults and infants but it starts as a new born(Cure Tay Sachs Fundation). How does this disease happen you may ask? According to The National Human Genone Institute, it explains the following. Tay Sachs is a genetic disorder that develops because the hexosaminidase enzyme doesn’t exist in the victim’s blood cycle ( Michael Pusaeri 2007) .This enzyme is a fatty substance (Cure Tay Sach Foundaion) that has

Genetic Disease Diagnosis, Screening and Treatment Advocacy and Decision Making in Genetics Competencies for Contemporary Nursing Issues (GNT1) Juanita Allen Janette Barney Western Governor 's University Task 3 724.2.5-03-08 724.2.6-02-09 Mr. and Mrs. Trosack have recently been told through chorionic villus testing, that their unborn child has Tay Sachs disease.As the case manager there should be several appropriate members identified for an interdisciplinary team to obtain information

Gene Therapy of Tay-Sachs Using a Modified Adenovirus Akash J. Patel Abstract: Tay Sach’s disease results in an accumulation of lipids in the brain’s nerve cells. The underlying cause of Tay-Sachs disease is a mutation in a gene that codes for a lytic enzyme known as Hexosaminidase A (Hex A). Tay-Sachs as well as other lipid storage diseases are incurable, but we believe that gene therapy has the potential for widespread correction of the lipid storage defect in humans by means of the cross-correction

Some of the general symptoms of the disease can be characterized by hind limb spasticity, weight loss, tremors, abnormal posture with lordosis, and possibility of visual impairment. Muscle weakness, clasping of the limbs, and myoclonic twitches of the head that can be onset late in the disease. Research of the GM2 ganglioside has revealed that storage of the fatty substance varies a large Tay-Sachs Disease2 amount in different regions, but the majority resides in the pyriform cortex, hippocampus

Tay Sachs disease is a life threatening disease that is passed down through families. Anyone can be a carrier of Tay Sachs, but is not common in the general population. The disease is most common in the Jewish population. 1 in every 27 members is a carrier of the disease. 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 typically

you could not chew to eat? Tay Sachs disease is a genetic disorder that cause five year death penalty. Before you are born Tay Sachs is where your 15th chromosome is broken and can not cover itself up. The first physical symptom to appear when born is to have a red dot on the inside of your eye, from there it get worse until after five years they could be paralyzed and lose all hearing and vision. There is no cure or way to deal with Tay Sachs. Discovered first by Warren Tay on Accident he was a british