se-atlas

Mapping of Health Care Providers
for People with Rare Diseases

Zentrum für Seltene Neurologische Erkrankungen

Decription of facility

Director / Spokesperson
Prof. Dr. Albert C. Ludolph
Information
Care facility for adults and children
Decription

Das Zentrum für Seltene Neurologische Erkrankungen befasst sich mit allen diagnostischen und therapeutischen Aspekten von seltenen Erkrankungen auf neurologischem Fachgebiet, mit
Schwerpunkten in der entsprechenden Versorgung von Patienten mit neurodegenerativen
Motoneuronerkrankungen, Patienten mit neurodegenerativen Bewegungsstörungen und Patienten mit seltenen Demenzformen. Hinsichtlich der Betreuung von Patienten mit Erkrankungen des
Skelettmuskels besteht eine enge Verbindung und teilweise inhaltliche und organisatorische
Überlappung mit dem Zentrum für Seltene Skelettmuskelerkrankungen.

Care provisions

This facility offers the following
  • Participation in registries
  • Genetic counselling
  • Clinical studies / research
  • Diagnostic
  • Therapy
  • Contact person for patients with an unclear diagnosis

Contact

Prof. Dr. Albert C. Ludolph
0731 1771201
zse@uniklinik-ulm.de
Website

https://www.uniklinik-ulm.de/zentrum-fuer-seltene-erkrankungen/fachzentren.html

Address

Oberer Eselsberg 45
89081 Ulm

Calculate route

Languages

Germany.png Deutsch
United_Kingdom.png Englisch

European Reference Network 1

Mentioned by the following facilities 1

Preview of the assigned diseases 9

Foix-Chavany-Marie syndrome Progressive muscular atrophy Juvenile amyotrophic lateral sclerosis X-linked distal hereditary motor neuropathy Young adult-onset distal hereditary motor neuropathy Madras motor neuron disease Amyotrophic lateral sclerosis type 4 Autosomal recessive distal hereditary motor neuropathy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Motor neuron disease Autosomal recessive lower motor neuron disease with childhood onset Distal hereditary motor neuropathy type 1 Distal hereditary motor neuropathy type 2 Distal hereditary motor neuropathy type 5 Distal hereditary motor neuropathy, Jerash type Amyotrophic lateral sclerosis Infantile-onset ascending hereditary spastic paralysis Juvenile primary lateral sclerosis Distal hereditary motor neuropathy type 7 Primary lateral sclerosis Huntington disease Amyotrophic lateral sclerosis-parkinsonism-dementia complex Kennedy disease 17q11 microdeletion syndrome Behavioral variant of frontotemporal dementia Atypical progressive supranuclear palsy syndrome Classic progressive supranuclear palsy syndrome Logopenic progressive aphasia Infectious encephalitis ITM2B amyloidosis Progressive supranuclear palsy-parkinsonism syndrome Frontotemporal dementia, right temporal atrophy variant Progressive supranuclear palsy-pure akinesia with gait freezing syndrome Progressive supranuclear palsy-corticobasal syndrome Posterior cortical atrophy Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Leigh syndrome Encephalitis Cerebral sinovenous thrombosis Monosomy 22q13 Moyamoya disease Moyamoya disease with early-onset achalasia MELAS Infantile bilateral striatal necrosis Neuromyelitis optica Robinow syndrome Multiple system atrophy, parkinsonian type Neurofibromatosis type 6 Noonan syndrome Progressive supranuclear palsy Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Multiple system atrophy, cerebellar type Cockayne syndrome Primary central nervous system vasculitis Primary progressive aphasia Corticobasal syndrome Prader-Willi syndrome Semantic dementia Frontotemporal degeneration with dementia Progressive non-fluent aphasia Dubowitz syndrome Neuronal intranuclear inclusion disease Subacute sclerosing leukoencephalitis Familial cerebral saccular aneurysm Infantile neuroaxonal dystrophy Frontotemporal dementia HERNS syndrome Seckel syndrome Smith-Lemli-Opitz syndrome Susac syndrome Watson syndrome Sporadic infantile bilateral striatal necrosis Familial infantile bilateral striatal necrosis Legius syndrome Aarskog-Scott syndrome Neurofibromatosis type 1 Neurofibromatosis type 2 Hereditary spastic paraplegia Reversible cerebral vasoconstriction syndrome

Provided care options 0

No available care options have been entered.
9.9445917317518448.42448955Zentrum für Seltene Neurologische Erkrankungen
Last updated: 03.11.2020