Question

TS is an inheritable disease mainly caused by a mutation in the SLITRK1 gene. This gene is located in the basal ganglia, the cortex, and the frontal lobes. The gene is located on chromosome 13 in position 31.1 and is important for the growth of nerve cells and their connections to other neurons. About 1 out of 360 children are diagnosed with TS from ages 6 to 17. Children who are caucasian, male, and between the ages of 12 to 17 are at a higher risk of developing TS. Out of all patients, only 37?

Answer 1

Tourette syndrome is a genetic disorder related to neurological problems that causes involuntary vocal sounds and movements. It is mainly caused by a mutation in the SLITRK1 gene located on chromosome 13 position 31.1. TS is more commonly diagnosed in caucasian, male children between the ages of 12 to 17.

Step-by-step explanation:

Tourette syndrome (TS) is a genetic disorder related to neurological problems. People with TS make involuntary vocal sounds and movements. The SLITRK1 gene, located on chromosome 13 position 31.1, is responsible for TS. It is an important gene for the growth of nerve cells and their connections to other neurons. TS is more commonly diagnosed in children who are caucasian, male, and between the ages of 12 to 17. About 1 out of 360 children in this age range are diagnosed with TS.