Panayiotopoulos syndrome

Panayiotopoulos syndrome (also known as PS) is a relatively common epilepsy syndrome that affects children aged between 3 and 6 years old. It is characterized by seizures, often occurring during sleep, and is typically outgrown by adolescence.

Symptoms[edit | edit source]

The primary symptom of Panayiotopoulos syndrome is seizures. These seizures often occur during sleep and can last for several minutes to a few hours. The seizures are often accompanied by autonomic symptoms such as changes in skin color, heart rate, and pupil size. Other symptoms may include nausea, vomiting, and eye deviation.

Causes[edit | edit source]

The exact cause of Panayiotopoulos syndrome is unknown. However, it is believed to be genetic in nature, as it often runs in families. Some researchers believe that it may be related to a mutation in the CHRNA4 gene.

Diagnosis[edit | edit source]

Diagnosis of Panayiotopoulos syndrome is based on the child's symptoms and medical history. A neurological examination may be performed to rule out other conditions. Electroencephalogram (EEG) testing is often used to confirm the diagnosis.

Treatment[edit | edit source]

Treatment for Panayiotopoulos syndrome typically involves antiepileptic drugs (AEDs). These medications can help to control seizures and reduce their frequency. In some cases, a ketogenic diet may be recommended.

Prognosis[edit | edit source]

The prognosis for children with Panayiotopoulos syndrome is generally good. Most children outgrow the condition by adolescence and do not experience long-term neurological effects.

See also[edit | edit source]

Panayiotopoulos syndrome Resources
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