Klinik für Kinderheilkunde I - Bereich Neuropädiatrie am Universitätsklinikum Essen Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Acute encephalopathy with inflammation-mediated status epilepticus
Atypical Rett syndrome
Atypical autism
Benign occipital epilepsy
Benign partial infantile seizures
Cerebral diseases of vascular origin with epilepsy
Cerebral malformation with epilepsy
Childhood disintegrative disorder
Childhood-onset epilepsy syndrome
Chromosomal anomaly with epilepsy as a major feature
Continuous spikes and waves during sleep
Cryptogenic late-onset epileptic spasms
Dravet syndrome
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
Early-onset progressive encephalopathy with migrant continuous myoclonus
Epilepsy syndrome
Epilepsy with eyelid myoclonia
Epilepsy with myoclonic absences
Familial infantile myoclonic epilepsy
Familial partial epilepsy
Generalized epilepsy with febrile seizures-plus
Idiopathic hemiconvulsion-hemiplegia syndrome
Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
Infantile epilepsy syndrome
Infantile spasms syndrome
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Infectious disease with epilepsy
Inflammatory and autoimmune disease with epilepsy
Juvenile myasthenia gravis
Landau-Kleffner syndrome
Lennox-Gastaut syndrome
Metabolic diseases with epilepsy
Monogenic disease with epilepsy
Motor neuron disease
Muscular channelopathy
Myoclonic epilepsy in non-progressive encephalopathies
Myoclonic epilepsy of infancy
Myoclonic-astatic epilepsy
Neonatal epilepsy syndrome
Neurocutaneous syndrome with epilepsy
Neurometabolic disease
Neuromuscular disease
Neuromuscular junction disease
Non-specific early-onset epileptic encephalopathy
Perioral myoclonia with absences
Progressive myoclonic epilepsy
Progressive myoclonic epilepsy with dystonia
Rare developmental defect during embryogenesis
Rare disease with autism
Rare epilepsy
Rare pervasive developmental disorder
Reflex epilepsy
Rett syndrome
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
Rolandic epilepsy-speech dyspraxia syndrome
Skeletal muscle disease