Autosomal Dominant Partial Epilepsy with Auditory Features: Causes, Symptoms, and Treatment

Medically reviewed by Harsha Moole, MD, Internal Medicine. Last reviewed: October 2, 2026.

What kind of doctor treats Autosomal Dominant Partial Epilepsy with Auditory Features?

A neurologist usually treats this condition. Some neurologists focus even more narrowly on seizures and are called epileptologists. A primary care doctor can help coordinate care and arrange the referral. A direct primary care or concierge doctor can be a first stop for an evaluation and can refer you to a specialist when needed.

What it is

Autosomal dominant partial epilepsy with auditory features, often shortened to ADPEAF, is a rare form of epilepsy in which seizures start in one small part of the brain, usually the temporal lobe, the area near the ear that helps process sound and language. Autosomal dominant describes how it is passed down in families, partial means the seizure starts in one spot, and auditory features means many people hear sounds during their seizures.

Symptoms

The most common symptom is hearing something that is not really there when a seizure begins , buzzing, ringing, clicking, humming, or voices. Doctors call these auditory hallucinations. Some people also have trouble understanding spoken words during a seizure.

Many people have only these brief sound episodes, called simple partial seizures, and stay awake and aware. Others have bigger seizures that spread through the brain, causing confusion, repeated movements, or loss of awareness.

Causes and who gets it

ADPEAF is caused by a changed gene passed down in families; changes in a gene called LGI1 cause most cases. Because it is autosomal dominant, only one parent needs to pass on the changed gene. Seizures usually begin in the teens or early adulthood.

How doctors diagnose it

Doctors start by asking about symptoms and family history. An EEG records the brain's electrical activity and can show signs of epilepsy. An MRI scan rules out other causes. Genetic testing can confirm the diagnosis in many cases.

Treatment

ADPEAF is usually treated with daily anti-seizure medicines. Many people respond well, and some do especially well with a medicine called carbamazepine. With treatment, many people have few or no seizures.

When to see a doctor

See a doctor for unexplained episodes of hearing sounds that are not there, or any seizure. Seek emergency care if a seizure lasts more than five minutes, happens one after another, or if breathing does not return to normal afterward.

How a direct primary care or concierge doctor fits in

A direct primary care doctor is paid a flat monthly fee instead of billing insurance; a concierge doctor usually charges more and often works alongside insurance. Either can be a steady partner for someone with ADPEAF, offering longer appointments and help with refills and side effects. They do not usually manage epilepsy on their own, so they refer the patient to a neurologist and stay involved between specialist visits.

Common questions

Can ADPEAF be cured?

There is no cure, but the condition is often well controlled with medicine. Many people have few or no seizures once treatment starts.

Will my children get it?

Because it is autosomal dominant, each child of a parent with the changed gene has a one in two chance of inheriting it. Not everyone who inherits the gene has seizures. Genetic counseling can help families understand the details.

Is it dangerous?

Most people with ADPEAF live normal lives with treatment. Any seizure that causes loss of awareness carries some safety risks, so doctors give guidance about driving, swimming, and other activities.

Do I need genetic testing?

Genetic testing can confirm the diagnosis and help other family members. It is not always required if the story and tests are typical. A neurologist or genetic counselor can explain the options.

Sources

  1. MedlinePlus - Autosomal dominant epilepsy with auditory features
  2. Epilepsy Foundation - What Is Epilepsy?

Medical Disclaimer

This content is for general educational and informational purposes only and is not medical advice. It is not a substitute for professional medical advice, diagnosis, or treatment, and reading it does not create a doctor-patient relationship. Always seek the advice of your physician or another qualified health provider with any questions about a medical condition, and never disregard or delay seeking professional advice because of something you read here. If you think you may have a medical emergency, call 911 (or your local emergency number) immediately.