Unverricht-Lundborg Syndrome


Baltic Myoclonic Epilepsies

Baltic Myoclonic Epilepsy

Baltic Myoclonus

Baltic Myoclonus Epilepsies

Baltic Myoclonus Epilepsy

Disease, Unverricht

Disease, Unverricht-Lundborg

Diseases, Unverricht

Diseases, Unverricht-Lundborg

Epilepsies, Baltic Myoclonic

Epilepsies, Baltic Myoclonus

Epilepsy, Baltic Myoclonic

Epilepsy, Baltic Myoclonus

Epilepsy, Mediterranean Myoclonic

Epilepsy, Progressive Myoclonic 1

Epilepsy, Progressive Myoclonic 1a

Epilepsy, Progressive Myoclonic Type 1

Epilepsy, Progressive Myoclonus 1

Lundborg Unverricht Syndrome

Lundborg-Unverricht Syndrome

Mediterranean Myoclonic Epilepsy

Myoclonic Epilepsies, Baltic

Myoclonic Epilepsy of Unverricht and Lundborg

Myoclonic Epilepsy, Baltic

Myoclonic Epilepsy, Mediterranean

Myoclonus Epilepsies, Baltic

Myoclonus Epilepsy, Baltic

Myoclonus Progressive Epilepsy of Unverricht and Lundborg

Myoclonus, Baltic

Progressive Myoclonus Epilepsy 1

Progressive Myoclonus Epilepsybaltic Myoclonic Epilepsy

Syndrome, Lundborg-Unverricht

Syndrome, Unverricht-Lundborg

Unverricht Disease

Unverricht Diseases

Unverricht Lundborg Disease

Unverricht Lundborg Syndrome

Unverricht-Lundborg Disease

Unverricht-Lundborg Diseases

An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, dysarthria, and intention tremor. Myoclonic seizures are severe and continuous, and tend to be triggered by movement, stress, and sensory stimuli. The age of onset is between 8 and 13 years, and the condition is relatively frequent in the Baltic region, especially Finland. (From Menkes, Textbook of Child Neurology, 5th ed, pp109-110)

See Also