Sleep-related hypermotor epilepsy

From WikiMD.org
Jump to navigation Jump to search

Sleep-related hypermotor epilepsy (SHE; pronounced: /ˈsliːp rɪˈleɪtɪd haɪpərˈmoʊtər ˈɛpɪˌlɛpsi/), formerly known as Nocturnal Frontal Lobe Epilepsy (NFLE), is a type of epilepsy that causes abnormal movements during sleep. The etymology of the term comes from the Greek words "hypnos" (sleep), "hyper" (excessive), "motor" (movement), and "epilepsia" (seizure).

Overview

SHE is characterized by the occurrence of seizures during sleep, which can range from simple jerking of the limbs to complex sequences of movements, such as kicking, punching, or even running. These seizures are typically brief, lasting less than 2 minutes, but can occur multiple times during a night's sleep.

Causes

The exact cause of SHE is unknown, but it is believed to be related to a dysfunction in the frontal lobe of the brain, which controls movement. Some studies suggest a genetic component, with mutations in the CHRNA4, CHRNB2, and KCNQ2 genes being associated with the condition.

Diagnosis

Diagnosis of SHE is based on the patient's symptoms and sleep history, as well as electroencephalogram (EEG) findings. An overnight sleep study, or polysomnography, may also be performed to capture the seizures and analyze the brain's activity during sleep.

Treatment

Treatment for SHE typically involves the use of antiepileptic drugs (AEDs), such as carbamazepine, oxcarbazepine, or lamotrigine. In some cases, surgery may be considered if the seizures are localized to a specific area of the brain and are not controlled by medication.

See also

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski