SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik Hoher Meißner

Description of facility

Director / Spokesperson
Dr. med. Carsten Schröter, Dr. med. Volker Stück
Information
Care facility for adults
Description
Die Klinik Hoher Meißner ist eine Fachklinik für Physikalisch-Rehabilitative Medizin und Schmerzbehandlung mit den Fachrichtungen Orthopädie, Traumatologie (AHB) und Neurologie (AHB, Phase C und D) in 37242 Bad Sooden-Allendorf. Schwerpunkte bestehen in der Neurologischen Abteilung für Patienten mit neuromuskulären Erkrankungen, wie Muskeldystrophien, spinale und neurale Muskeldystrophien, Post-Polio-Syndrom, entzündliche neuromuskuläre Erkrankungen, ebenso die spastische Spinalparalyse. Ein weiterer Schwerpunkt besteht in der Behandlung der Dystonien. Schwerpunkte in der Orthopädischen Abteilung bestehen in der Behandlung u.a. von Patienten mit Fibromyalgie, Morbus Sudeck, sowie Patienten mit Thalidomid-Folgen (Contergan). Ansprechpartner sind Frau Dr. Brückner (Chefärztin Orthopädie), Herr Dr. Schröter (Chefarzt Neurologie), Aufnahmebüro Frau Mülverstedt.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Information
05652 550
info@reha-klinik.de
Website http://www.reha-klinik.de/

Address

Hardtstraße 36
37242 Bad Sooden-Allendorf

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Mentioned by the following facilities 2

Preview of the assigned diseases 6

Andersen-Tawil syndrome Autosomal recessive spastic paraplegia type 35 Autosomal spastic paraplegia type 18 Mutilating hereditary sensory neuropathy with spastic paraplegia Autosomal dominant spastic paraplegia type 3 Autosomal recessive spastic paraplegia type 5A Autosomal dominant spastic paraplegia type 4 Autosomal dominant spastic paraplegia type 8 Autosomal dominant spastic paraplegia type 6 Allan-Herndon-Dudley syndrome Autosomal dominant spastic paraplegia type 10 Autosomal dominant spastic paraplegia type 12 Autosomal recessive spastic paraplegia type 14 Autosomal dominant spastic paraplegia type 13 Severe intellectual disability and progressive spastic paraplegia X-linked spastic paraplegia type 16 Autosomal recessive spastic paraplegia type 15 Autosomal dominant spastic paraplegia type 19 Autosomal recessive spastic paraplegia type 21 Autosomal recessive spastic paraplegia type 20 Autosomal recessive spastic paraplegia type 24 Autosomal recessive spastic paraplegia type 23 Autosomal recessive spastic paraplegia type 26 Autosomal recessive spastic paraplegia type 25 Autosomal recessive spastic paraplegia type 28 Postpoliomyelitis syndrome Autosomal recessive spastic paraplegia type 27 Autosomal spastic paraplegia type 30 X-linked pure spastic paraplegia Autosomal dominant spastic paraplegia type 31 Autosomal recessive spastic paraplegia type 39 Spastic paraplegia-glaucoma-intellectual disability syndrome Pure or complex autosomal dominant spastic paraplegia Autosomal recessive spastic paraplegia type 11 Pure or complex X-linked spastic paraplegia Pure or complex autosomal recessive spastic paraplegia Macrocephaly-spastic paraplegia-dysmorphism syndrome Autosomal dominant spastic paraplegia type 41 MT-ATP6-related mitochondrial spastic paraplegia Amyotrophic lateral sclerosis Autosomal recessive spastic paraplegia type 55 Duchenne and Becker muscular dystrophy Autosomal recessive spastic paraplegia type 43 Spastic paraplegia type 7 Spastic paraplegia type 2 Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Autosomal recessive spastic paraplegia type 54 Hereditary spastic paraplegia Autosomal recessive spastic paraplegia type 46 Autosomal dominant spastic paraplegia type 42 Duchenne muscular dystrophy MASA syndrome Becker muscular dystrophy Autosomal recessive spastic paraplegia type 44 Autosomal recessive spastic paraplegia type 45 Menkes disease Complex regional pain syndrome type 1 Complex regional pain syndrome type 2 X-linked spastic paraplegia type 34 Spastic paraplegia-optic atrophy-neuropathy syndrome Autosomal dominant spastic paraplegia type 37 Autosomal recessive spastic paraplegia type 56 Autosomal recessive spastic paraplegia type 53 Thalidomide embryopathy Genetic periodic paralysis Alpers-Huttenlocher syndrome Autosomal recessive spastic paraplegia type 32 Autosomal recessive spastic paraplegia type 48

Provided care options 3

# Contact person
1
Neurologischer Behandlungsschwerpunkt
Dr. med. Carsten Schröter

05652 55861
Email
Website

2
Orthopädischer Behandlungsschwerpunkt
Dr. med. Volker Stück

05652 55821
Email
Website

3
Behandlungsschwerpunkt Motorische Störungen - Rehabilitation
Dr. med. Volker Stück

05652 55821
Email
Website

9.955247146251.2754557Klinik Hoher Meißner
Last updated: 22.11.2022