Autosomal Dominant Partial Epilepsy with Auditory FeaturesSymptoms, Doctors, Treatments, Advances & More
Autosomal Dominant Partial Epilepsy with Auditory Features Overview
Learn About Autosomal Dominant Partial Epilepsy with Auditory Features
- Autosomal dominant partial epilepsy with auditory features
- ADLTE
- ADPEAF
- Autosomal dominant lateral temporal lobe epilepsy
- ETL1
St. Vincent Neurosurgery
Javier Echeverri is a Neurologist in Billings, Montana. Dr. Echeverri has been practicing medicine for over 47 years and is rated as a Distinguished provider by MediFind in the treatment of Autosomal Dominant Partial Epilepsy with Auditory Features. His top areas of expertise are Essential Tremor, Parkinson's Disease, Movement Disorders, Epilepsy with Myoclonic-Atonic Seizures, and Deep Brain Stimulation. Dr. Echeverri is currently accepting new patients.
Ballad Health Medical Associates Neurology
Arvo Kanna, MD, became a neurologist because he was deeply fascinated by the complexities of the human brain. “My job is like piecing together a puzzle, where I use a patient’s medical history along with examination and tests to find an accurate diagnosis.” Dr. Kanna believes that a strong patient-physician relationship is one of the most important tools a doctor can have. “Creating a personal connection is essential,” he says. “It lets the patient know that you genuinely care.”. Dr. Kanna is rated as an Advanced provider by MediFind in the treatment of Autosomal Dominant Partial Epilepsy with Auditory Features. His top areas of expertise are Autosomal Dominant Partial Epilepsy with Auditory Features, Epilepsy Juvenile Absence, Absence Seizure, and Memory Loss.
Advocate Medical Group Neurology
Christopher Fahey is a Sleep Medicine provider in Park Ridge, Illinois. Dr. Fahey is rated as an Advanced provider by MediFind in the treatment of Autosomal Dominant Partial Epilepsy with Auditory Features. His top areas of expertise are Headache, Seizures, Memory Loss, and Autosomal Dominant Partial Epilepsy with Auditory Features.
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center


