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[edit | edit source]
The most common symptoms of Wild Man Syndrome include:
- Severe intellectual disability
- Epilepsy
- Autism
- Distinctive facial features
Causes[edit | edit source]
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[edit | edit source]
Diagnosis of Wild Man Syndrome is based on the presence of characteristic clinical features. Genetic testing can confirm the diagnosis.
Treatment[edit | edit source]
There is currently no cure for Wild Man Syndrome. Treatment is supportive and based on the symptoms present in each individual.
Prognosis[edit | edit source]
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[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD
