Tay-Sachs disease is a rare genetic disorder, which occurs in the formation of fat cells, particularly in brain and nerve cells (neurons). Causing mental retardation and physical barriers to the development of normal accompanied by seizures, blindness, paralysis and death. There is no specific treatment for this disorder.
This disease consists of several types, whereas the focus in this article is Tay-Sachs Infantil Acute most frequently found.
People with this disease have enzyme levels heksosamidase A (hex A) is low compared to those working to solve this normal.Enzim gangliosida (a fat) in body cells. These fatty compounds are gradually buried and cause damage to brain cells and nerves so that these cells do not function properly.
READ MORE - Tay-Sachs Disease Causes Mental Retardation
This disease consists of several types, whereas the focus in this article is Tay-Sachs Infantil Acute most frequently found.
People with this disease have enzyme levels heksosamidase A (hex A) is low compared to those working to solve this normal.Enzim gangliosida (a fat) in body cells. These fatty compounds are gradually buried and cause damage to brain cells and nerves so that these cells do not function properly.