SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik und Poliklinik für Kinder- und Jugendmedizin - Pädiatrie I am Universitätsklinikum Halle

Description of facility

Director / Spokesperson
PD Dr. med. Jessica Höll
Information
Care facility for children
Description

Die Universitätsklinik und Poliklinik für Pädiatrie I ist mit ihrem Pädiatrisch-Onkologischen Zentrum und dem Perinatalzentrum Level 1 sowie einer breit aufgestellten, spezialärztlichen Allgemeinpädiatrie als Maximalversorger in der Pädiatrie für die Stadt Halle und die Region des südlichen Sachsen-Anhalt einschliesslich der angrenzenden Städte und Gemeinden anderer Bundesländer tätig.

In enger Verzahnung von Patientenversorgung und wissenschaftlicher Arbeit widmet sich diese Klinik der Erforschung, Erkennung und Behandlung schwerer und auch seltener Erkrankungen des Kindes- und Jugendalters. 

Diese Klinik betreut akut und chronisch kranke Patienten von der Geburt bis zum jungen Erwachsenenalter, d.h. unreife und reife Neugeborene, Säuglinge, Kleinkinder, Schulkinder und Jugendliche. 

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Sekretariat
0345 557 2388
0345 557 2389
kinderklinik@uk-halle.de
Website https://www.medizin.uni-halle.de/einrichtungen/kliniken-und-departments/department-fuer-operative-und-konservative-kinder-und-jugendmedizin/paediatrie-i

Address

Ernst-Grube-Straße 40
06120 Halle (Saale)

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 3

Preview of the assigned diseases 15

Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Eosinophilic fasciitis Cryoglobulinemic vasculitis Oligoarticular juvenile idiopathic arthritis Unspecified juvenile idiopathic arthritis Systemic-onset juvenile idiopathic arthritis Hemophilia Intermittent hydrarthrosis Mixed autoinflammatory and autoimmune syndrome Polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Rare systemic or rheumatological disease of childhood Pyogenic autoinflammatory syndrome of childhood Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Enthesitis-related juvenile idiopathic arthritis Periodic fever syndrome of childhood Granulomatous autoinflammatory syndrome of childhood Bleeding disorder in hemophilia A carriers Gorham-Stout disease Unclassified autoinflammatory syndrome of childhood Rare hemorrhagic disorder STAT3-related early-onset multisystem autoimmune disease Bleeding disorder in hemophilia B carriers Overlapping connective tissue disease Immunoglobulin A vasculitis Rare pediatric vasculitis Idiopathic juvenile osteoporosis Rare coagulation disorder Juvenile idiopathic arthritis Rare pediatric systemic disease Unclassified vasculitis Secondary neonatal autoimmune disease Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Unexplained long-lasting fever/inflammatory syndrome Cogan syndrome Sweet syndrome Juvenile dermatomyositis Rare thrombotic disease of hematologic origin Sarcoidosis Behçet disease Pediatric Castleman disease Severe hemophilia B STING-associated vasculopathy with onset in infancy Anti-neutrophil cytoplasmic antibody-associated vasculitis Pediatric systemic lupus erythematosus Moderate hemophilia B Severe hemophilia A Mild hemophilia B Hemophilia B Hypocomplementemic urticarial vasculitis Hemophilia A Systemic sclerosis Moderate hemophilia A Hajdu-Cheney syndrome Mild hemophilia A Juvenile polymyositis Progeria-associated arthropathy Autoimmune interstitial lung disease-arthritis syndrome Secondary vasculitis Vasculitis due to ADA2 deficiency Kawasaki disease Takayasu arteritis Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Reactive arthritis PLCG2-associated antibody deficiency and immune dysregulation Autoinflammatory syndrome of childhood Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Niemann-Pick disease type C Carbamoyl-phosphate synthetase 1 deficiency Argininosuccinic aciduria Ornithine transcarbamylase deficiency Carnitine palmitoyl transferase 1A deficiency Short chain acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Medium chain acyl-CoA dehydrogenase deficiency Adenylosuccinate lyase deficiency Mucopolysaccharidosis type 1 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 3 Phenylketonuria Citrullinemia type I

Provided care options 3

# Contact person
1
Kinderhämostaseologisches Zentrum
Dr. med. Caspar Kühnöl

0345 5572053
Email
Website
Sprechzeiten nach Vereinbarung.

2
Kinderrheumatologischen Ambulanz
Dr. med. Regina Hühn; Dr. med. Alexander Kühn

0345 5572053
Email
Website
Sprechzeiten nach Vereinbarung.

3
Sprechstunde für angeborene Stoffwechselerkrankungen
Dr. med. Marcus Stange

0345 5572053
Email
Website
Sprechzeiten: Mo - Fr 8:00 - 16:00 Uhr.
This consultation offers genetic counselling.

11.93665160036362151.50197945Klinik und Poliklinik für Kinder- und Jugendmedizin - Pädiatrie I am Universitätsklinikum Halle
Last updated: 14.09.2023