SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Zentrum für seltene neurologische Erkrankungen am Universitätsklinikum Schleswig-Holstein, Campus Kiel

Description of facility

Director / Spokesperson
PD Dr. med. Frank Leypoldt, Prof. Dr. Kirsten Zeuner (Stellvertretung)
Information
Care facility for adults and children
Description
In den Sprechstunden des Instituts für Neurogenetik und der Klinik für Neurologie werden in Zusammenarbeit mit der Klinik für Psychiatrie Patienten mit Bewegungsstörungen und neuropsychiatrischen Erkrankungen diagnostiziert und behandelt. Einige dieser Erkrankungen sind selten, für diese werden Spezialsprechstunden und besondere genetische Untersuchungen angeboten. Für diese speziellen Fragestellungen kooperiert das Institut mit weiteren Einrichtungen der Universität wie dem Institut für Humangenetik, der Kinderklinik und der Klinik für Neurochirurgie.

Care provisions

This facility offers the following
  • Genetic counselling
  • Diagnostic
  • Therapy

Contact

Terminvergabe
0431 50023900
0431 50023904
ambulanz.neurologie.kiel@uksh.de
Website https://www.uksh.de/zse-kiel/Struktur+_+Fachzentren/Fachzentrum+f%C3%BCr+seltene+neurologische+Erkrankungen.html

Secondary Contact

Neurologische Privatambulanz
0431 50023801
0431 50023904

Address

Arnold-Heller-Straße 3
24105 Kiel
Haus D (Neurozentrum)

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Preview of the assigned diseases 6

Early-onset generalized limb-onset dystonia Miscellaneous movement disorder due to neurodegenerative disease Spinocerebellar ataxia with oculomotor anomaly Rare dystonia Rare inborn errors of metabolism Huntington disease Frontotemporal neurodegeneration with movement disorder Generalized isolated dystonia Rare genetic hyperkinetic movement disorder Disorder of tyrosine metabolism Paroxysmal dyskinesia Persistent combined dystonia Combined dystonia Autosomal recessive dopa-responsive dystonia Neurometabolic disease Myoclonus-dystonia syndrome Atypical progressive supranuclear palsy syndrome Primary dystonia, DYT21 type Progressive supranuclear palsy Rare genetic neurological disorder Rare parkinsonian disorder Rare neurodegenerative disease Huntington disease-like syndrome Primary myoclonus Rare disorder with dystonia and other neurologic or systemic manifestation Autosomal dominant cerebellar ataxia type I Combined cervical dystonia Spinocerebellar ataxia type 8 Focal, segmental or multifocal dystonia Genetic neurodegenerative disease Rare dementia Rare paroxysmal movement disorder Progressive supranuclear palsy-parkinsonism syndrome Disorder of phenylalanin or tyrosine metabolism Disorder of amino acid and other organic acid metabolism Hereditary ataxia Rapid-onset dystonia-parkinsonism Genetic neurodegenerative disease with dementia Psychogenic movement disorders Autosomal dominant cerebellar ataxia Rare genetic movement disorder Multiple system atrophy Paroxysmal dystonia Neurodegenerative disease with dementia X-linked dystonia-parkinsonism Rare genetic parkinsonian disorder Huntington disease-like syndrome due to C9ORF72 expansions Rare parkinsonian syndrome due to genetic neurodegenerative disease Rare neurologic disease with psychiatric involvement Rare movement disorder Rare genetic dystonia Rare ataxia Multiple system atrophy, parkinsonian type Hereditary episodic ataxia Paroxysmal kinesigenic dyskinesia Autosomal dominant dopa-responsive dystonia Rare genetic myoclonus Isolated dystonia Rare hyperkinetic movement disorder Dopa-responsive dystonia
10.14288732743867554.3304953Zentrum für seltene neurologische Erkrankungen am Universitätsklinikum Schleswig-Holstein, Campus Kiel
Last updated: 12.09.2023