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 practicing medicine in Billings, Montana. Dr. Echeverri is rated as a Distinguished provider by MediFind in the treatment of Autosomal Dominant Partial Epilepsy with Auditory Features. He is also highly rated in 26 other conditions, according to our data. His clinical expertise encompasses Essential Tremor, Parkinson's Disease, Movement Disorders, Epilepsy with Myoclonic-Atonic Seizures, and Deep Brain Stimulation.
Trinity Clinic
John Hueter is a Neurologist practicing medicine in Texarkana, Texas. Dr. Hueter is rated as a Distinguished provider by MediFind in the treatment of Autosomal Dominant Partial Epilepsy with Auditory Features. He is also highly rated in 20 other conditions, according to our data. His clinical expertise encompasses Migraine, Memory Loss, Autosomal Dominant Partial Epilepsy with Auditory Features, and Epilepsy. Dr. Hueter is board certified in American Board Of Psychiatry And Neurology. Dr. Hueter is currently accepting new patients.
Avera Brain & Spine Institute — Plaza 2
William Rossing is a Neurologist practicing medicine in Sioux Falls, South Dakota. Dr. Rossing is rated as a Distinguished provider by MediFind in the treatment of Autosomal Dominant Partial Epilepsy with Auditory Features. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Drug Induced Dyskinesia, Essential Tremor, Autosomal Dominant Partial Epilepsy with Auditory Features, and Seizures. Dr. Rossing is board certified in American Board Of Psychiatry And Neurology - Neurology. Dr. Rossing is currently accepting new patients.
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center


