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What causes BECTS epilepsy?

What causes BECTS epilepsy?

The EEG pattern that is seen in BECTS is inherited in an autosomal dominant pattern. Several different possible gene mutations seem to cause this pattern. Only about a quarter of children who inherit this EEG pattern have seizures, so it seems likely that other genes or environmental factors also influence BECTS.

What does a benign Rolandic seizure look like?

Benign rolandic epilepsy is characterized by twitching, numbness or tingling of the child’s face or tongue, and may interfere with speech and cause drooling. Seizures spread from one area of the brain and become generalized.

Is Rolandic epilepsy genetic?

Rolandic epilepsy (RE) is the most common type of childhood epilepsy-affecting more than 50,000 children in the United States-and has a complex genetic inheritance.

Is epilepsy linked to autism?

Yes, there is an association between epilepsy and autism. Children with autism are (a little) more likely to have epilepsy. Children with epilepsy are (a little) more likely to have autism. Seizures are the most common neurologic complication in ASD.

Where is the Rolandic part of the brain?

The seizures, sometimes referred to as sylvian seizures, start around the central sulcus of the brain (also called the centrotemporal area, located around the Rolandic fissure, after Luigi Rolando)….

Rolandic epilepsy
Specialty Neurology

How is Rolandic epilepsy diagnosed?

Doctors diagnose benign rolandic epilepsy based on the pattern of seizures. They also gather information from multiple tests: Electroencephalogram (EEG): By attaching a set of adhesive electrodes to the scalp, a technician records brain waves during this painless test. A neurologist interprets the EEG.

Where is the Rolandic area of brain?

[1] Most of the affected children usually outgrow this condition by puberty, hence the term “benign.”[2][3] The seizures originate in the Rolandic area of the brain (situated around the central sulcus of the brain, also called as centrotemporal area, located around the Rolandic fissure).

Is epilepsy a mental disease?

Epilepsy is not a mental illness. In fact, the vast majority of people living with epilepsy have no cognitive or psychological problem. For the most part, psychological issues in epilepsy are limited to people with severe and uncontrolled epilepsy.

Does Rolandic epilepsy go away?

Benign rolandic epilepsy is one form of epilepsy. With this condition, seizures affect the face and sometimes the body. As a result, the disorder causes problems for some children. It almost always disappears, though, by adolescence.

What is benign rolandic epilepsy (cects)?

The official modern name is “childhood epilepsy with centrotemporal spikes” or CECTS. Yet, many people still just use the term benign rolandic epilepsy to refer to this syndrome.

How is benign rolandic epilepsy (Bre) diagnosed?

As with other epilepsy syndromes, a diagnosis of benign Rolandic epilepsy (BRE) is based on history and confirmed with characteristic electroencephalogram (EEG) findings.[15] 

When do seizures stop in benign rolandic epilepsy?

In the majority of patients, the seizures stop on their own during adolescence. Seizures associated with benign rolandic epilepsy are usually brief — no more than two minutes in duration. They tend to occur infrequently and most often at night. The child may maintain full awareness while the seizure is happening.

What are the cardinal features of Rolandic epilepsy?

The cardinal features of Rolandic epilepsy are infrequent, often single, focal seizures consisting of: Hemifacial sensorimotor seizures are often entirely localised in the lower lip or spread to the ipsilateral hand. Motor manifestations are sudden, continuous or bursts of clonic contractions, usually lasting from a few seconds to a minute.