Exactly? Well, it is a dominate gene and an autosomal condition, so if you do get only one copy from one parent, you still have a 50% chance of getting it. Each affected person usually has one affected parent. There is a 50% chance that a child will inherit the mutated gene. Conditions that are autosomal dominant often have low penetrance, which means that although only one mutated copy is needed, and a relatively (25% or half of those who get the gene in Tourettes case) small proportion of those who inherit that mutation go on to develop the disease.
It is hereditary but can become apparent in kids with no family history of any neurological condition, however because it is caused by neurological structure rather than psychological issues it is difficult to get outside of hereditary conditions.
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It is caused by a deletion of chromosome 15, if inherited from the mother.
No, they originate from an inherited neurological disorder. You don't get to blame society for your messed-up genes.
Tourettes Syndrom is a condition in the Nervous System
scientist have found that there might be a mutation gene in a person with tourettes syndrome, but it is still unknown
Yes, 'tourettes' is correct.--- Not if you refer to the syndrome. Then it is spelled Tourette's
Yosef's Genes
This combination XXY produces a male child with Klinefelter's Syndrome.
Klinefelter's Syndrome results when a person has XXY chromosomes (an extra X chromosome). The main effects of this are hypogonadism and reduced fertility.
Over 100,000 (one hundred thousand) people have Tourettes Syndrome in the United States of America Over 100,000 (one hundred thousand) people have Tourettes Syndrome in the United States of America
This combination XXY produces a male child with Klinefelter's Syndrome.
This combination XXY produces a male child with Klinefelter's Syndrome.
Most cases of down syndrome are not inherited. Translocation Down syndrome can be inherited.