Tay-sachs Disease

Tay-Sachs Disease Tay-Sachs Disease can be a very compelling disease because it attacks children and babies most sensitively. This disease is very rare and fatal. Tay Sachs is a hereditary disorder in which a large amount of fat fat is formed in many nerve cells called Ganglioside GM2. Infants who are Tay-sachs but not carriers appear to develop normally in a few months after birth, but mental and physical abilities are severely compromised as nerve cells are swollen with fatty substances .

Tessa disease Disease disease is a fatal disease affecting the human nervous system. Tay-Sachs disease is a hereditary disease transmitted from the parent to offspring because there is no protein called hexosaminidase A in the body. Protein hexosaminidase A contributes to chemical degradation of gangliosides and other phospholipids found in nerve tissue. Tay-Sachs disease is caused by defective genes on chromosome 15. According to McKenzie (2009), Tay-Sachs disease is caused by excessive accumulation of ganglioside cell membranes in nerve cells in the brain, resulting in aminohexosaminidase A activity deficient protein. Tay-Sachs disease usually develops when a baby enters the womb, develops rapidly after birth, and dies when that baby is 4-6 years old. In the months after birth, infants with Taza's disease develop more complications and die within 4 to 6 years. The treatment of disease is not known

Juvenile Tay-Sachs disease. Juvenile Tay - Sachs disease is rarer than other forms of Tay - Sachs and is usually seen first in children between 2 and 10 years of age. People with Tay-Sachs disease develop cognitive and motor skills, dysarthria, difficulty swallowing, ataxia, and paralysis. Death usually occurs between 5 and 15 years old. Adult / late-onset Tay-Sachs disease. The rare form of this disease, known as adult onset or delayed onset, is the first symptom in thirties or forties. Contrary to other forms, late-onset Tay - Sachs disease is not usually fatal, as it may result in ineffective progress. It is often misdiagnosed. It is characterized by gait instability and progressive neurological deterioration