Congenital Bilateral Perisylvian Syndrome (CBPS) is a rare neurological disorder that affects the development of the brain. It is characterized by a combination of physical, cognitive, and behavioral symptoms. The most common physical symptoms include seizures, hypotonia (low muscle tone), and facial asymmetry. Cognitive symptoms may include intellectual disability, language delays, and learning disabilities. Behavioral symptoms may include hyperactivity, impulsivity, and difficulty with social interactions. Treatment typically includes medications, physical and occupational therapy, and speech and language therapy.

The symptoms of Congenital Bilateral Perisylvian Syndrome vary from person to person, but may include:

- Delayed speech and language development
- Difficulty understanding language
- Poor motor coordination
- Poor fine motor skills
- Poor gross motor skills
- Poor balance
- Seizures
- Abnormal EEG
- Abnormal MRI
- Abnormal CT scan
- Abnormal facial features
- Abnormal head shape
- Abnormal eye movements
- Abnormal hand movements
- Abnormal gait
- Abnormal posture
- Abnormal reflexes
- Abnormal muscle tone
- Abnormal breathing patterns
- Abnormal swallowing patterns
- Abnormal sleep patterns
- Abnormal behavior
- Intellectual disability

Congenital Bilateral Perisylvian Syndrome (CBPS) is a rare neurological disorder that is caused by a genetic mutation. The exact cause of the mutation is unknown, but it is believed to be caused by a combination of genetic and environmental factors. Some of the known causes of CBPS include chromosomal abnormalities, such as trisomy 21 (Down syndrome), and certain genetic syndromes, such as Smith-Lemli-Opitz syndrome. In some cases, the cause of CBPS is unknown.

Treatment for Congenital Bilateral Perisylvian Syndrome is typically focused on managing the individual’s symptoms. This may include physical, occupational, and speech therapy to help improve motor skills, communication, and social skills. Medications may also be prescribed to help manage seizures, anxiety, and other behavioral issues. Surgery may be recommended in some cases to help improve the individual’s quality of life. Additionally, genetic counseling may be recommended to help families understand the condition and its implications.

1. Genetic mutations: Mutations in the FOXG1 gene are the most common cause of Congenital Bilateral Perisylvian Syndrome.

2. Family history: A family history of Congenital Bilateral Perisylvian Syndrome increases the risk of the condition.

3. Maternal age: Women over the age of 35 are more likely to have a child with Congenital Bilateral Perisylvian Syndrome.

4. Environmental factors: Exposure to certain environmental toxins or infections during pregnancy may increase the risk of Congenital Bilateral Perisylvian Syndrome.

At this time, there is no known cure for Congenital Bilateral Perisylvian Syndrome. However, there are medications and therapies that can help manage the symptoms associated with the condition. These include medications to help control seizures, physical therapy to help improve motor skills, and speech therapy to help improve communication. Additionally, there are a variety of assistive devices and adaptive strategies that can help individuals with Congenital Bilateral Perisylvian Syndrome to better manage their daily activities.