5,10-Methylenetetrahydrofolate Reductase Deficiency and Myoclonic Epilepsy

Investigators from the Children's Hospital of Philadelphia, PA, and McGill University, Montreal, Quebec, CA, report an adolescent learning-disabled girl who presented at age 14 years with an epilepsy syndrome initially diagnosed as juvenile myoclonic epilepsy.

Saved in:
Bibliographic Details
Main Authors: J Gordon Millichap, John J Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2014-09-01
Series:Pediatric Neurology Briefs
Subjects:
Online Access:https://www.pediatricneurologybriefs.com/articles/116
Tags: Add Tag
No Tags, Be the first to tag this record!