SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
ARX-related epileptic encephalopathy Acute disseminated encephalomyelitis Bickerstaff brainstem encephalitis CDKL5-deficiency disorder Cerebral diseases of vascular origin with epilepsy Cerebral malformation with epilepsy Chromosomal anomaly with epilepsy as a major feature Classic paraneoplastic limbic encephalitis Continuous spikes and waves during sleep Dravet syndrome Early infantile epileptic encephalopathy Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome Epilepsy syndrome Epileptic encephalopathy with global cerebral demyelination Febrile infection-related epilepsy syndrome Hyperekplexia Hypothalamic hamartomas with gelastic seizures Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Infectious disease with epilepsy Inflammatory and autoimmune disease with epilepsy Isaacs syndrome KCNQ2-related epileptic encephalopathy Lethal neonatal spasticity-epileptic encephalopathy syndrome Limbic encephalitis Limbic encephalitis associated with antibodies to cell membrane antigens Limbic encephalitis with DPP6 antibodies Limbic encephalitis with LGI1 antibodies Limbic encephalitis with caspr2 antibodies Limbic encephalitis with nCMAgs antibodies Limbic encephalitis with neurexin-3 antibodies Metabolic diseases with epilepsy Monogenic disease with epilepsy Morvan syndrome NMDA receptor encephalitis Neurocutaneous syndrome with epilepsy Non-herpetic acute limbic encephalitis Non-paraneoplastic limbic encephalitis Non-specific early-onset epileptic encephalopathy Paraneoplastic limbic encephalitis Posttransplant acute limbic encephalitis Progressive encephalomyelitis with rigidity and myoclonus Pyridoxal phosphate-responsive seizures Rare epilepsy Tuberous sclerosis complex