Three Indian siblings affected with progressive myoclonic epilepsy due to unverricht-Lundborg disease

• Main Authors: Kavita Srivastava (Author), Bina Mahendrasinh Thakor (Author), Shuvendu Roy (Author), Surekha Rajadhyaksha (Author), Chaitanya Datar (Author)
• Format: Book
• Published: Wolters Kluwer Medknow Publications, 2022-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Background: Progressive myoclonus epilepsy (PME) is a group of heterogeneous genetic disorders characterized by action myoclonus, epileptic seizures, and progressive neurologic deterioration with onset of symptoms in adolescence and adulthood. Unverricht-Lundborg disease (ULD) is the most common typ...