There is no cure for Ashersona's Syndrome, but medications can be used to help manage symptoms. These medications may include stimulants, antidepressants, antipsychotics, and mood stabilizers. It is important to work with a doctor to find the best medication and dosage for each individual.

1. Family history of autoimmune diseases
2. Exposure to environmental toxins
3. Genetic predisposition
4. Stressful life events
5. Vitamin D deficiency
6. Exposure to certain medications
7. Exposure to certain infections
8. Exposure to certain foods

The treatment for Ashersona's Syndrome is focused on managing the symptoms. This may include medications to help with attention, impulsivity, and hyperactivity, as well as psychotherapy to help with behavior and social skills. Other treatments may include occupational therapy, speech therapy, and educational interventions.

Ashersona Syndrome is a rare genetic disorder caused by a mutation in the gene that codes for the protein filamin A. This mutation affects the development of the brain, leading to a range of physical and cognitive impairments. The exact cause of the mutation is unknown, but it is believed to be inherited in an autosomal recessive pattern.

The main symptoms of Ashersona's Syndrome are:

1. Attention Deficit Hyperactivity Disorder (ADHD)
2. Impulsivity
3. Hyperactivity
4. Poor concentration
5. Poor organizational skills
6. Poor social skills
7. Poor academic performance
8. Low self-esteem
9. Anxiety
10. Depression
11. Sleep disturbances
12. Aggression
13. Oppositional behavior

Ashersona's Syndrome is a rare genetic disorder that affects the nervous system. It is characterized by a combination of physical and mental symptoms, including developmental delays, intellectual disability, seizures, and behavioral problems. It is caused by a mutation in the gene that codes for the protein called Ashersona.