Many people have been suffering from different types of diseases and disorders in which many failed to survive and fight against their specific health conditions. In fact, many people are not yet aware of the existence of rare forms of diseases which have been suffered by certain individuals from various parts of the world. One of them is the Tay Sachs Disease which can eventually change the lives of the affected persons. Find out about it and be able to share the most useful information if you know somebody else who also suffer from this condition.
What is Tay Sachs Disease?
Tay Sachs refers to the rare form of disease which takes place in the nervous system of a person. This is actually a disease that is inherited from any family members and can be passed to the next generations. This is very dangerous and is deadly.
This is also often described as the genetic disorder of lipid storage which is fatal and causes dangerous fatty substance amount to form in nerve tissues and cells.
Basically, this disease is due to the insufficiency of hexosaminidase A, which is the protein utilized for breaking down the nerve tissue chemicals. The harmful chemicals have been brought by gangliosides in which these damage the nerve tissue which starts in the person’s brain. Tay Sachs usually causes blindness, seizures, paralysis, deafness, dementia and other symptoms. An affected person may die at 4 years old. This is also possible for the affected persons to notice symptoms and acquire this disease later, however, this condition less likely happens. In fact, there were no records indicating the famous individuals who acquired Tay-Sachs disease.
Cures and Treatments
Anybody can carry Tay-Sachs disease. To deal with this disease, the parents should be carriers. The symptoms have no specific time when they are going to appear. This disease develops in any life stages, but it usually occurs during infantile stages. Tay Sachs disease does not actually choose a type of person since the race, age or gender do not matter at all.
Whenever a person is suspected to acquire this disease, the doctors are going to conduct physical examinations and take a look at the historical background of the family. This is how Tay Sachs disease is being diagnosed. When the tests had been proven as inconclusive, the blood enzyme analysis is conducted in order to determine if there is insufficiency in hexosaminidase A, along with eye examination.
During the eye examination, when the “cherry red spots” had been discovered in macula, it proves that the person is positive of Tay-Sachs disease. The truth is that there are no solutions or treatments for this disease. Doctors state that the only treatment to treat Tay-Sachs patients is to allow them feel great comfort. This can be done through letting them join groups with the similar situations to relieve their stress.
Tay-Sachs disease was actually discovered by Bernard Sachs and Warren Tay during the late nineteenth century. They were not working together but they both described and discovered the disease as well as ways to diagnose it.
