Myoclonic epilepsy, Hartung type is a neurological condition primarily characterized by seizure activity that can include sudden, brief muscle jerks....

Myoclonic epilepsy in infancy is a neonatal and infantile epilepsy syndrome characterized by myoclonic seizures that typically begin between 6 and 18...

Myoclonic epilepsy in non-progressive encephalopathies is a rare epilepsy syndrome that primarily affects infants and young children. It is characteri...

Myoclonic epilepsy, juvenile, 2 (also known as EJM2) is a neurological condition primarily characterized by seizures that involve sudden, brief muscle...

Myoclonic epilepsy of Lafora 1 is a neurological disorder that falls under the progressive myoclonus epilepsies and primarily affects the nervous syst...

Myoclonic epilepsy of Lafora 2 is a neurodegenerative disorder that primarily affects the central nervous system and is characterized by seizures and...

Myoclonus-cerebellar ataxia-deafness syndrome is a condition defined by the presence of myoclonus, cerebellar ataxia, and sensorineural hearing loss....

Myoclonus-dystonia syndrome is a rare movement disorder characterized by mild to moderate dystonia and lightning-like myoclonic jerks. The condition h...

Myoclonus, familial is a rare genetic movement disorder that predominantly affects adults and is characterized by brief, jerky, involuntary movements...

Myofascial pain syndrome is a musculoskeletal condition characterized by muscle pain and the presence of trigger points in the soft tissues. The pain...

Myofibrillar myopathy is a group of muscle disorders that affect both skeletal and cardiac muscles. It is primarily characterized by slowly progressiv...

Myofibrillar myopathy 1 is a genetic skeletal muscle disorder characterized by abnormal clumps of desmin and related proteins in muscle tissue, leadin...

Myofibrillar myopathy 2 is an inherited muscle disorder that primarily affects the skeletal muscles, particularly those of the distal limbs. It is cau...

Myofibrillar myopathy 3 is a rare late adult‐onset neuromuscular disorder that primarily affects distal skeletal muscles, leading to progressive weakn...

Myofibrillar myopathy 4, also known as late-onset distal myopathy, Markesbery-Griggs type, is a rare, genetic, non-dystrophic disorder that primarily...

Myofibrillar myopathy 5 is a type of muscle filaminopathy, a rare disorder affecting the skeletal muscles that is characterized by slowly progressive...