Tourette's syndrome is a neurological disorder, which involves involuntary body movements or Tics. There are two types of Tics, motor/physical and vocal. This paper will cover many aspects of Tourette's syndrome; including the history of the disease, the discovered of the disease, the genetics involved with the disorder, the diagnosis of the disease, and the effects of the disease on families. George Gils de la Tourette's a French doctor and biologist discovered Tourette's syndrome in 1885 (Landau 21). He was observing patients with unexplained repetitive movements and could not find any preexisting condition that would cause these symptoms. After extensive research he concluded that this disorder had not been documented before, so he named it Tourette's syndrome, after himself. Tourette’s syndrome is a neurological disorder; it is inherited from a parent’s dominant gene, causing different symptoms among different family members. It is not known on which chromosome the disease is located. There is a 50% chance that one will pass this trait on to his/her offspring with each pregnancy (Shimberg 64). There is no prenatal testing that can be done before a child is born to determine if the child has the disease. Unlike other genetic disorders or disease Tourette's is not in the blood. Therefore testing will not give any indication of whether or not a child will develop Tourette's. Cases of the disease show males are burden with the disease three to four times more often then females. There is a 15% chance that the disorder will evolve during childhood. Both motor and vocal tics become less frequent with age but unfortunately will never Thursfield 2disappear. The U.S. Medical Survey estimates that 100,000 people have full blown Tourette's syndrome, and there are up to 300,0000 have minor undiagnosed cases.Tourette's Syndrome causes an individual to lose control of body movement resulting in repetitive actions and verbalizati...
