SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik für Neuropädiatrie und Sozialpädiatrisches Zentrum am Klinikum Kassel

Description of facility

Director / Spokesperson
Prof. Dr. med. Bernd Wilken
Information
Care facility for children
Description
In der Neuropädiatrie und dem sozialpädiatrischen Zentrum werden seit 1974 Kinder und Jugendliche untersucht, behandelt und betreut, die eine Erkrankung des Nervensystems, des Gehirns, der Muskulatur oder eine Entwicklungsstörung haben. Um diesem Anspruch gerecht zu werden arbeiten viele verschiedene Berufsgruppen unter kinderärztlicher Leitung interdisziplinär zusammen.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Sekretariat
0561 9803096
0561 9806946
wilken@klinikum-kassel.de
Website http://www.klinikum-kassel.de/index.php?parent=1311

Address

Mönchebergstraße 41-43
34125 Kassel
Zentrum für Frauen- und Kindermedizin, Haus F

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 1

Preview of the assigned diseases 1

Psychogenic movement disorders Rolandic epilepsy-speech dyspraxia syndrome 15q13.3 microdeletion syndrome Benign partial infantile seizures Benign occipital epilepsy Childhood-onset epilepsy syndrome Infantile epilepsy syndrome Neonatal epilepsy syndrome Progressive myoclonic epilepsy Adolescent-onset epilepsy syndrome Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Dravet syndrome Epilepsy syndrome Lennox-Gastaut syndrome Neurocutaneous syndrome with epilepsy Neuromuscular disease Tetrasomy 12p Benign adult familial myoclonic epilepsy Rare parkinsonian disorder Landau-Kleffner syndrome Angelman syndrome Malignant migrating focal seizures of infancy New-onset refractory status epilepticus Chromosomal anomaly with epilepsy as a major feature Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes W syndrome Ring chromosome 14 syndrome Acute encephalopathy with inflammation-mediated status epilepticus Ring chromosome 20 syndrome Cerebral malformation with epilepsy Inflammatory and autoimmune disease with epilepsy Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Fragile X syndrome Miscellaneous movement disorder due to neurodegenerative disease Epileptic encephalopathy with global cerebral demyelination Inherited congenital spastic tetraplegia Familial acute necrotizing encephalopathy Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome 1p36 deletion syndrome PEHO-like syndrome Generalized epilepsy with febrile seizures-plus Non-specific early-onset epileptic encephalopathy PEHO syndrome Rare epilepsy Central nervous system malformation Rare movement disorder Rare choreic movement disorder Moynahan syndrome Rare neuroinflammatory or neuroimmunological disease Neuroleptic malignant syndrome Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Miller-Dieker syndrome Kleefstra syndrome due to 9q34 microdeletion Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Wolf-Hirschhorn syndrome Rare myoclonus Severe neonatal-onset encephalopathy with microcephaly Oculocerebrocutaneous syndrome CNTNAP2-related developmental and epileptic encephalopathy Familial infantile myoclonic epilepsy Rare paroxysmal movement disorder Progressive myoclonic epilepsy with dystonia Action myoclonus-renal failure syndrome Early infantile epileptic encephalopathy Motor stereotypies Idiopathic hemiconvulsion-hemiplegia syndrome Early myoclonic encephalopathy DEND syndrome Myoclonic epilepsy of infancy Rare dystonia Myoclonic epilepsy in non-progressive encephalopathies Epilepsy with myoclonic absences Perioral myoclonia with absences Myoclonic-astatic epilepsy Benign idiopathic neonatal seizures Early-onset progressive encephalopathy with migrant continuous myoclonus Hyperekplexia Febrile infection-related epilepsy syndrome Infantile spasms-broad thumbs syndrome Familial partial epilepsy Cryptogenic late-onset epileptic spasms Epilepsy with eyelid myoclonia Reflex epilepsy Familial congenital mirror movements Benign familial neonatal epilepsy Infantile spasms syndrome Epilepsy-telangiectasia syndrome Continuous spikes and waves during sleep Benign focal seizures of adolescence

Provided care options 1

# Contact person
1
Spezialambulanz für Neuropädiatrie mit Epileptologie (DGfE e.V. zertifiziert)
Prof. Dr. med. Bernd Wilken

0561 9803096
Email
Website
Termine nach telefonischer Vereinbarung.

9.50950920581817851.32796361891037Klinik für Neuropädiatrie und Sozialpädiatrisches Zentrum am Klinikum Kassel
Last updated: 22.05.2023