Tourette syndrome is a neurological disorder characterized by involuntary movements and vocalizations called tics. The exact cause is not fully understood, but it is believed to involve a combination of genetic, environmental, and neurobiological factors. Abnormal levels of neurotransmitters, particularly dopamine, in specific areas of the brain may also play a role in the development of the disorder. Family history can increase the likelihood of developing Tourette syndrome, indicating a genetic component.
No. Tourette's syndrome is a neurological disorder, typically caused by an abnormally structured basal ganglia and prefrontal cortex. It may also be related to levels of noradrenalin, seratonin and dopamine in the brain. It is not a mental disorder. Evidence suggests that individuals with Tourette's without comorbid conditions have a higher-than-predicted* IQ (based on a statistical model taking into account their age, family history and background), and may be more skilled at grammer and native-language skills. No studies on mathematical skills have been performed.
No. Tourette's syndrome is a neurological disorder, typically caused by an abnormally structured basal ganglia and prefrontal cortex. It may also be related to levels of noradrenalin, seratonin and dopamine in the brain. It is not a mental disorder. Evidence suggests that individuals with Tourette's without comorbid conditions have a higher-than-predicted* IQ (based on a statistical model taking into account their age, family history and background), and may be more skilled at grammer and native-language skills. No studies on mathematical skills have been performed.
well. . .maybe you should look, instead of being lazy and asking the world. . K? thanks(: peace <3
Strattera (atomoxetine) is generally considered safe for individuals with a seizure disorder, but caution is advised. While it is not contraindicated, it's essential to consult a healthcare provider before starting the medication, as they can assess your specific condition and medical history. Monitoring for any changes in seizure frequency or severity is also important when starting Strattera. Always follow your doctor's guidance regarding medication management.
Hutchinson-Gilford Progeria Syndrome is considered an autosomal dominant condition, which means one copy of the altered gene in each cell is sufficient to cause the disorder. The condition results from new mutations in the LMNA gene, and almost always occurs in people with no history of the disorder in their family.
Strattera (atomoxetine) is primarily used to treat ADHD and is not a stimulant. For individuals with bipolar disorder, especially bipolar II, it's essential to consult a healthcare provider before using Strattera, as it can potentially affect mood stability. While some may tolerate it well, others could experience mood swings or exacerbation of symptoms. A healthcare professional can evaluate the risks and benefits based on the individual's specific situation and history.
Strattera (atomoxetine) is not commonly associated with causing seizures. However, in rare cases, it may lower the seizure threshold, particularly in individuals with a history of seizures or certain medical conditions. It's important for anyone taking Strattera to discuss their medical history with their healthcare provider to assess any potential risks. If a patient experiences seizures while on Strattera, they should seek immediate medical attention.
earlier in history people who had tourettes or some kind of neurological disorder were thought to be possessed by the devil but the first man to actually believe it was something other than that was George Albert Edouard Giles De La Tourette in 1884
Asperger's Syndrome was discovered by Hans Asperger in 1944.
Morquio syndrome, a genetic disorder, is inherited in an autosomal recessive manner, meaning a child must receive two mutated copies of the gene (one from each parent) to be affected. To reduce the risk of transferring the condition, prospective parents can undergo genetic counseling and testing, especially if there is a family history of the syndrome. If both parents are carriers, they may consider options such as in vitro fertilization with preimplantation genetic diagnosis to select embryos without the disorder.
Canavan of history of the disorder