SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik und Poliklinik für Kinder- und Jugendmedizin am Universitätsklinikum Hamburg-Eppendorf

Description of facility

Director / Spokesperson
Prof. Dr. med. Ania C. Muntau
Information
Care facility for children
Description
Das interdisziplinäre Team der Klinik und Poliklinik für Kinder- und Jugendmedizin mit insgesamt 352 Mitarbeitern steht bei Fragen oder Sorgen rund um die Kindergesundheit gerne zur Verfügung. Die Ärzte und Pflegekräfte der Spezialabteilungen bieten ambulante und stationäre Versorgungsoptionen an.

Als Universitätskinderklinik ist das interdisziplinäre Team nicht nur für alle Fragen der kindlichen Gesundheit zuständig sondern fühlt sich in besonderer Weise auch für Kinder und Jugendliche verantwortlich, die von schweren, komplexen und seltenen Erkrankungen betroffen sind.

Care provisions

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

Contact

Information
040 741020400
040 741020404
kinderklinik@uke.de
Website https://www.uke.de/kliniken-institute/kliniken/kinder-und-jugendmedizin/index.html

Address

Martinistraße 52
20246 Hamburg
Gebäude O47

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

European Reference Network 1

Mentioned by the following facilities 3

Preview of the assigned diseases 13

Thrombotic microangiopathy CLN1 disease Kawasaki disease Pelizaeus-Merzbacher-like disease due to AIMP1 mutation Cree leukoencephalopathy Ovarioleukodystrophy Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Infantile neuronal ceroid lipofuscinosis Pelizaeus-Merzbacher disease Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Autoinflammatory syndrome of childhood Alagille syndrome due to a JAG1 point mutation OBSOLETE: CLN3 disease Cryoglobulinemic vasculitis Eosinophilic fasciitis Unspecified juvenile idiopathic arthritis Muckle-Wells syndrome PLCG2-associated antibody deficiency and immune dysregulation Oligoarticular juvenile idiopathic arthritis CLN2 disease Hereditary periodic fever syndrome CLN5 disease Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies CLN9 disease Nasu-Hakola disease Congenital or early infantile CACH syndrome CLN6 disease Congenital neuronal ceroid lipofuscinosis Neonatal adrenoleukodystrophy Mixed autoinflammatory and autoimmune syndrome Microscopic polyangiitis Relapsing polychondritis Hypomyelination with atrophy of basal ganglia and cerebellum Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Periodic fever syndrome of childhood Fabry disease Alagille syndrome Juvenile or adult CACH syndrome Metachromatic leukodystrophy, late infantile form Rare systemic or rheumatological disease of childhood Hypomyelination-congenital cataract syndrome Psoriasis-related juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Allan-Herndon-Dudley syndrome Metachromatic leukodystrophy, juvenile form Infantile onset panniculitis with uveitis and systemic granulomatosis 4H leukodystrophy Metachromatic leukodystrophy, adult form Familial Mediterranean fever Hyperimmunoglobulinemia D with periodic fever Gorham-Stout disease Idiopathic recurrent pericarditis Pelizaeus-Merzbacher disease, classic form Sterile multifocal osteomyelitis with periostitis and pustulosis Overlapping connective tissue disease Pelizaeus-Merzbacher disease in female carriers Krabbe disease Unknown leukodystrophy Primary glomerular disease Infantile Krabbe disease Unexplained periodic fever syndrome of childhood Pelizaeus-Merzbacher disease, transitional form Late-infantile/juvenile Krabbe disease Granulomatosis with polyangiitis Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Adult Krabbe disease Drug-induced vasculitis Infantile Refsum disease Null syndrome Zellweger syndrome Alexander disease type I Unclassified vasculitis Odontoleukodystrophy Metachromatic leukodystrophy Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Juvenile dermatomyositis Peroxisomal acyl-CoA oxidase deficiency JMP syndrome Pediatric Castleman disease Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome Pediatric systemic lupus erythematosus CANDLE syndrome Secondary glomerular disease Pelizaeus-Merzbacher-like disease Mixed connective tissue disease Pelizaeus-Merzbacher-like disease due to GJC2 mutation Hypocomplementemic urticarial vasculitis Mild Canavan disease Spastic paraplegia type 2 CACH syndrome Pelizaeus-Merzbacher-like disease due to HSPD1 mutation Hajdu-Cheney syndrome Alagille syndrome due to 20p12 microdeletion Canavan disease Juvenile polymyositis Adrenomyeloneuropathy Adult-onset autosomal dominant leukodystrophy Leukodystrophy NLRP3-associated autoinflammatory disease Ravine syndrome CLN7 disease Leukoencephalopathy with mild cerebellar ataxia and white matter edema CADDS Late infantile CACH syndrome Reactive arthritis Severe Canavan disease Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Sarcoidosis X-linked adrenoleukodystrophy Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Postinfectious vasculitis Aicardi-Goutières syndrome Rare pediatric vasculitis Nakajo-Nishimura syndrome Alexander disease NLRP12-associated hereditary periodic fever syndrome Granulomatous autoinflammatory syndrome of childhood Peroxisome biogenesis disorder Juvenile idiopathic arthritis Unclassified autoinflammatory syndrome of childhood Polyarticular juvenile idiopathic arthritis Leukoencephalopathy-dystonia-motor neuropathy syndrome Mixed cryoglobulinemia type III Mixed cryoglobulinemia type II Proteasome-associated autoinflammatory syndrome Behçet disease Wilson disease Cerebrotendinous xanthomatosis Cystic leukoencephalopathy without megalencephaly Hypomyelination with brain stem and spinal cord involvement and leg spasticity PFAPA syndrome Pelizaeus-Merzbacher disease, connatal form Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease Juvenile neuronal ceroid lipofuscinosis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Sweet syndrome Progressive cavitating leukoencephalopathy Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Eosinophilic granulomatosis with polyangiitis Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Cogan syndrome Tumor necrosis factor receptor 1 associated periodic syndrome Unexplained long-lasting fever/inflammatory syndrome Alexander disease type II Takayasu arteritis Blau syndrome CLN10 disease Alagille syndrome due to a NOTCH2 point mutation Refsum disease STXBP1-related encephalopathy X-linked cerebral adrenoleukodystrophy CINCA syndrome Majeed syndrome DITRA Primary Sjögren syndrome Localized scleroderma Non-infectious anterior uveitis Early-onset sarcoidosis CLN8 disease PAPA syndrome Genetic glomerular disease Late infantile neuronal ceroid lipofuscinosis Rare pediatric systemic disease Alpha-1-antitrypsin deficiency Pyogenic autoinflammatory syndrome of childhood Vasculitis due to ADA2 deficiency Giant cell arteritis Megalencephalic leukoencephalopathy with subcortical cysts CREST syndrome Leukoencephalopathy with bilateral anterior temporal lobe cysts Familial cold urticaria Idiopathic juvenile osteoporosis Anti-neutrophil cytoplasmic antibody-associated vasculitis Immunoglobulin A vasculitis

Provided care options 6

# Contact person
1
Sprechstunde für pädiatrische Nephrologie
Dr. med. Jun Oh

040 741051200
Email
Website
Sprechzeiten: Mo 8:30 - 12:00 Uhr und 14:00 - 17:00 Uhr, Di, Do, Fr 8:30 - 12:00 Uhr sowie Mi 8:30 - 12:00 Uhr und 14:00 - 18:00 Uhr nach Vereinbarung.

2
Sprechstunde für Kinder- und Jugendrheumatologie
Dr. med. Fabian Speth, Dr. med. Anja Fröhlich

040 741020400
Email
Website
Sprechzeiten: Mo 13:00 - 18:00 Uhr, Di 8:00 Uhr - 12:00 Uhr sowie 14:00 - 16:00 Uhr, Do 8:00 Uhr - 11:00 Uhr und Fr 8:00 - 13:00 Uhr.

3
Sprechstunde für neuronale Ceroid-Lipofuszinosen- und Leukodystrophie-Krankheiten
Dr. med. Angela Schulz, Dr. med. Annette Bley

040 741020440
Email
Website
Sprechzeiten nach Vereinbarung.

4
Sprechstunde für Kinder und Erwachsene mit Morbus Fabry
PD Dr. med. Nicole Muschol

040 741053714
Email
Website
Sprechzeiten nach Vereinbarung.

5
Sprechstunde für pädiatrische Gastroenterologie und Hepatologie
PD Dr. med. Jun Oh, Dr. med. Daniel Tegtmeyer, Dr. med. Jan Beime

040 741020400
Email
Website
Sprechzeiten: Mo und Di 8:30 - 11:30 Uhr, Mi und Do 8:30 - 11:30 Uhr sowie 14:30 - 15:30 Uhr, Fr 9:00 - 11:30 Uhr nach Vereinbarung.

6
Sprechstunde für Neuropädiatrie
PD Dr. med. Jonas Denecke

040 741020400
Email
Website
Sprechzeiten: Mo u Do 08:00 - 13:00 Uhr, 14:00 - 16:00 Uhr, Di u Fr 08:00 - 13:00 Uhr, Mi 10:00 - 13:00 Uhr nach Vereinbarung.

9.9787809658844253.59183499819678Klinik und Poliklinik für Kinder- und Jugendmedizin am Universitätsklinikum Hamburg-Eppendorf
Last updated: 03.01.2024