Thyroxine-Induced Absences in JME
Abstract
A patient with juvenile myoclonic epilepsy (JME), manifested as absences at age 10 and myoclonic jerking and generalized tonic clonic seizures at age 15, was treated successfully with primidone at the King Fahad National Guard Hospital, Riyadh, Saudi Arabia.
DOI: https://doi.org/10.15844/pedneurbriefs-10-9-9 | Journal eISSN: 2166-6482
Language: English
Page range: 70 - 70
Published on: Sep 1, 1996
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 1996 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.