Wild man syndrome

Wild Man Syndrome is a rare genetic disorder characterized by severe intellectual disability, epilepsy, autism, and distinctive facial features. The syndrome is caused by mutations in the SYNGAP1 gene.

Symptoms

The most common symptoms of Wild Man Syndrome include:

• Severe intellectual disability
• Epilepsy
• Autism
• Distinctive facial features

Causes

Wild Man Syndrome is caused by mutations in the SYNGAP1 gene. This gene provides instructions for making a protein that is involved in the development and function of nerve cells in the brain.

Diagnosis

Diagnosis of Wild Man Syndrome is based on the presence of characteristic clinical features. Genetic testing can confirm the diagnosis.

Treatment

There is currently no cure for Wild Man Syndrome. Treatment is supportive and based on the symptoms present in each individual.

Prognosis

The prognosis for individuals with Wild Man Syndrome varies. Some individuals may have a normal lifespan, while others may have a shortened lifespan due to complications of the disorder.

See also

• Genetic disorder
• Intellectual disability
• Epilepsy
• Autism

References

Wild man syndrome Resources
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