5,10-Methylenetetrahydrofolate Reductase Deficiency and Myoclonic Epilepsy

Abstract

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.

Keywords

• dentatorubro-pallidoluysian atrophy
• progressive myoclonic epilepsy
• unverricht-lundborg