epilepsy, familial temporal lobe, 1

An autosomal dominant condition caused by mutation(s) in the LGI1 gene, encoding leucine-rich glioma-inactivated protein 1. It is characterized by partial seizures originating in the temporal lobe and often accompanied by auditory sensory manifestations.

What is epilepsy, familial temporal lobe, 1?

epilepsy, familial temporal lobe, 1 is a medical condition. A condition is a disease, disorder, or abnormal state that affects the body or mind. This page provides educational information only and is not a diagnosis.

If you think you may have epilepsy, familial temporal lobe, 1, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with epilepsy, familial temporal lobe, 1

Bilateral tonic-clonic seizureBilateral tonic-clonic seizure with focal onsetFocal aware seizureFocal clonic seizureFocal impaired awareness seizureFocal sensory seizure with olfactory featuresFocal sensory seizure with visual features

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.