Myoclonic Epilepsy Myopathy Sensory Ataxia

Myoclonic Epilepsy Myopathy Sensory Ataxia

Myoclonic epilepsy myopathy sensory ataxia is a rare neuromuscular disorder characterised by myoclonic seizures, muscle weakness, and issues with coordination and balance. Its symptoms typically manifest in childhood or adolescence. This condition often results from mitochondrial DNA mutations and requires multidisciplinary management for optimal care and quality of life.