Epilepsiezentrum Kork Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Angelman syndrome
Angelman syndrome due to maternal 15q11q13 deletion
Angelman syndrome due to paternal uniparental disomy of chromosome 15
Atypical Rett syndrome
Benign familial infantile epilepsy
Benign familial neonatal-infantile seizures
Benign infantile focal epilepsy with midline spikes and waves during sleep
Benign infantile seizures associated with mild gastroenteritis
Benign non-familial infantile seizures
Benign partial epilepsy of infancy with complex partial seizures
Benign partial epilepsy with secondarily generalized seizures in infancy
Benign partial infantile seizures
Distal duplication 15q
Dravet syndrome
Early-onset progressive encephalopathy with migrant continuous myoclonus
Familial infantile myoclonic epilepsy
Generalized epilepsy with febrile seizures-plus
Idiopathic hemiconvulsion-hemiplegia syndrome
Infantile convulsions and choreoathetosis
Infantile epilepsy syndrome
Infantile spasms syndrome
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Inverted duplicated chromosome 15 syndrome
Lennox-Gastaut syndrome
Myoclonic epilepsy in non-progressive encephalopathies
Myoclonic epilepsy of infancy
Progressive myoclonic epilepsy with dystonia
STXBP1-related encephalopathy
SYNGAP1-related developmental and epileptic encephalopathy
Severe neonatal-onset encephalopathy with microcephaly
Sturge-Weber syndrome