Related Experiment Video
Updated: Aug 7, 2026

Behavioral and Locomotor Measurements Using an Open Field Activity Monitoring System for Skeletal Muscle Diseases
Published on: September 29, 2014
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
C Pizzanelli1, M Mancuso, R Galli
1Neurophysiopathology Unit, Hospital Lotti, Via Roma 180, I-56025, Pontedera, and Department of Neuroscience, University of Pisa, Italy.
Abstract:
Autosomal recessive limb girdle muscular dystrophies (LGMD) type 2A are a group of disorders characterised by progressive involvement of proximal limb girdle muscles and caused by changes in the CAPN3 gene. Involvement of tissues other than the skeletal muscle has not been reported so far. Here we describe the unusual association of LGMD2A and idiopathic generalised epilepsy in a 14-year-old girl.
Related Concept Videos
Epilepsy ll: Types
Satellite Stem Cells and Muscular Dystrophy
Alterations in Muscle Tone ll
Seizures: Classification
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
Alterations in Muscle Tone lll
Sex-linked Disorders

