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