se-atlas

Mapping of Health Care Providers
for People with Rare Diseases

Klinik für Kinder- und Jugendmedizin am Universitätsklinikum Tübingen

Decription of facility

Director / Spokesperson
Prof. Dr. med. Rupert Handgretinger
Information
Care facility for children
Decription

Als Klinik für Kinder- und Jugendmedizin der Eberhard Karls Universität, Universitätsklinikum Tübingen, bietet die Klinik hochmoderne Krankenversorgung, innovative Forschung und kompetente Lehre und Ausbildung. Kinder sind keine kleinen Erwachsenen und brauchen daher spezialisierte medizinische Betreuung. Die fünf Fachabteilungen der Kinderklinik arbeiten eng zusammen und gewährleisten so eine kindgerechte und umfassende Betreuung.

Care provisions

This facility offers the following
  • Social / legal advice
  • Clinical studies / research
  • Diagnostic
  • Therapy

Contact

Information
07071 2983781
Website

http://www.medizin.uni-tuebingen.de/kinder/de/

Address

Hoppe-Seyler-Straße 1
72076 Tübingen

Calculate route

Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 3

Mentioned by the following facilities 1

Preview of the assigned diseases 7

Spina bifida-hypospadias syndrome Polyarticular juvenile idiopathic arthritis Nasu-Hakola disease X-linked adrenoleukodystrophy Neonatal adrenoleukodystrophy Congenital or early infantile CACH syndrome Autosomal dominant polycystic kidney disease Juvenile or adult CACH syndrome Spina bifida cystica Late infantile CACH syndrome Aicardi-Goutières syndrome Hypomyelination with atrophy of basal ganglia and cerebellum CADDS Progressive cavitating leukoencephalopathy Psoriasis-related juvenile idiopathic arthritis Hypomyelination-congenital cataract syndrome Leukoencephalopathy with bilateral anterior temporal lobe cysts Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Transient neonatal myasthenia gravis Alexander disease Pelizaeus-Merzbacher disease, connatal form Allan-Herndon-Dudley syndrome Metachromatic leukodystrophy, juvenile form Leukoencephalopathy with mild cerebellar ataxia and white matter edema Total spina bifida cystica Metachromatic leukodystrophy, late infantile form Cervical spina bifida cystica Pelizaeus-Merzbacher disease, classic form Hypomyelinating leukodystrophy with or without oligondontia and/or hypogonadism Metachromatic leukodystrophy, adult form STAT3-related early-onset multisystem autoimmune disease Hypomyelination with brain stem and spinal cord involvement and leg spasticity Symptomatic form of hemophilia A in female carriers Lumbosacral spina bifida cystica Infantile Krabbe disease Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Symptomatic form of hemophilia B in female carriers Kein Name gefunden Krabbe disease Overlapping connective tissue disease Pelizaeus-Merzbacher disease, transitional form Null syndrome Peroxisome biogenesis disorder Spina bifida aperta Late-infantile/juvenile Krabbe disease Von Willebrand disease Rare pediatric systemic disease Neurofibromatosis type 3 Pelizaeus-Merzbacher disease in female carriers Adult Krabbe disease Neurofibromatosis type 1 Von Willebrand disease type 2 Infantile Refsum disease Cerebrotendinous xanthomatosis Refsum disease Total spina bifida aperta Juvenile idiopathic arthritis Von Willebrand disease type 1 Neurofibromatosis-Noonan syndrome Alexander disease type I Zellweger syndrome Odontoleukodystrophy Alexander disease type II Unexplained long-lasting fever/inflammatory syndrome Lumbosacral spina bifida aperta Metachromatic leukodystrophy Secondary neonatal autoimmune disease Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Juvenile dermatomyositis Von Willebrand disease type 3 Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Neonatal antiphospholipid syndrome Cervical spina bifida aperta Sarcoidosis Severe Canavan disease Pelizaeus-Merzbacher-like disease Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome Pediatric Castleman disease Severe hemophilia B Neonatal autoimmune hemolytic anemia Diffuse cutaneous systemic sclerosis Pediatric systemic lupus erythematosus Mixed connective tissue disease Moderately severe hemophilia B Severe hemophilia A Mild Canavan disease Spastic paraplegia type 2 Neonatal dermatomyositis Hemophilia B Limited cutaneous systemic sclerosis Mild hemophilia B Hemophilia A Neonatal scleroderma Limited systemic sclerosis CACH syndrome Systemic sclerosis Autoimmune interstitial lung disease-arthritis syndrome Moderately severe hemophilia A CREST syndrome Pelizaeus-Merzbacher-like disease due to HSPD1 mutation Neonatal lupus erythematosus X-linked cerebral adrenoleukodystrophy Pelizaeus-Merzbacher-like disease due to GJC2 mutation Mild hemophilia A Juvenile polymyositis Isolated spina bifida Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Canavan disease Adrenomyeloneuropathy Adult-onset autosomal dominant leukodystrophy Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Kawasaki disease Ovarioleukodystrophy Ravine syndrome Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Leukoencephalopathy-dystonia-motor neuropathy syndrome Cree leukoencephalopathy Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Pelizaeus-Merzbacher disease Megalencephalic leukoencephalopathy with subcortical cysts Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Leukodystrophy Rheumatoid factor-negative juvenile idiopathic arthritis Cystic leukoencephalopathy without megalencephaly Eosinophilic fasciitis Oligoarticular juvenile idiopathic arthritis 17q11 microdeletion syndrome PLCG2-associated antibody deficiency and immune dysregulation Unspecified juvenile idiopathic arthritis Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Systemic-onset juvenile idiopathic arthritis Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies

Provided care options 6

# Contact person
1
Behandlungsschwerpunkt für Autoimmunerkrankungen und pädiatrische Rheumatologie
Prof. Dr. med. Jasmin Kümmerle-Deschner

07071 2984719
Website
Sprechzeiten: Mo 13:00 - 15:00 Uhr, Di - Do 8:30 - 11:30 Uhr sowie 13:00 - 15:00 Uhr und Fr 8:30 - 11:30 Uhr nach Vereinbarung.

2
Behandlungsschwerpunkt Gerinnung - Hämostaseologie
Information

07071 2983773
Email
Website
Sprechzeiten: Mo - Fr 14:00 - 15:00 Uhr nach Vereinbarung.

3
Behandlungsschwerpunkt Leukodystrophien
Prof. Dr. med. Marko Wilke

07071 2984735
Email
Website
Sprechzeiten nach Vereinbarung.

4
Behandlungsschwerpunkt Neurofibromatose
Dr. med. Michael Alber; Prof. Dr. med. Marko Wilke

07071 2983806
Email
Website
Sprechzeiten: Mo - Do 10:00 - 12:00 Uhr und 13:00 - 15:00 Uhr sowie Fr 10:00 - 12:00 Uhr und 13:00 - 14:30 Uhr nach Vereinbarung.

5
Behandlungsschwerpunkt Spina bifida
Dr. med. Michael Alber; Prof. Dr. med. Marko Wilke

07071 2983806
Email
Website
Sprechzeiten: Mo - Do 10:00 - 12:00 Uhr und 13:00 - 15:00 Uhr sowie Fr 10:00 - 12:00 Uhr und 13:00 - 14:30 Uhr nach Vereinbarung.

6
Behandlungsschwerpunkt Zystennieren
PD Dr. med. Marcus Weitz

07071 942560
Website
Sprechzeiten: Mo - Mi 8:00 - 13:00 Uhr sowie 14:30 - 15:30 Uhr und Do 8:00 - 12:30 Uhr nach Vereinbarung.

9.03915676430965448.53087682057437Klinik für Kinder- und Jugendmedizin am Universitätsklinikum Tübingen
Last updated: 15.09.2020