Klinik und Poliklinik für Kinder- und Jugendmedizin am Universitätsklinikum Dresden Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Adrenogenital syndrome
Aicardi-Goutières syndrome
Anti-neutrophil cytoplasmic antibody-associated vasculitis
Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome
Autoimmune interstitial lung disease-arthritis syndrome
Autoimmune thrombocytopenia
Autoinflammatory syndrome of childhood
Autosomal dominant polycystic kidney disease
Autosomal recessive polycystic kidney disease
Bleeding disorder in hemophilia A carriers
Bleeding disorder in hemophilia B carriers
CREST syndrome
Cogan syndrome
Cryoglobulinemic vasculitis
Diffuse cutaneous systemic sclerosis
Enthesitis-related juvenile idiopathic arthritis
Eosinophilic fasciitis
Full NF2-related schwannomatosis
Full schwannomatosis
Gorham-Stout disease
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
Mild hemophilia A
Mild hemophilia B
Mixed connective tissue disease
Moderate hemophilia A
Moderate hemophilia B
Neurofibromatosis type 1
Oligoarticular juvenile idiopathic arthritis
Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies
Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies
Overlapping connective tissue disease
PLCG2-associated antibody deficiency and immune dysregulation
Pediatric Castleman disease
Pediatric systemic lupus erythematosus
Polyarticular juvenile idiopathic arthritis
Progeria-associated arthropathy
Psoriasis-related juvenile idiopathic arthritis
Rare pediatric systemic disease
Rare pediatric vasculitis
Rare systemic or rheumatological disease of childhood
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
Sweet syndrome
Systemic sclerosis
Systemic-onset juvenile idiopathic arthritis
Takayasu arteritis
Unclassified vasculitis
Unexplained long-lasting fever/inflammatory syndrome
Unspecified juvenile idiopathic arthritis
Vasculitis due to ADA2 deficiency
Von Willebrand disease
Von Willebrand disease type 1
Von Willebrand disease type 2
Von Willebrand disease type 2A
Von Willebrand disease type 2B
Von Willebrand disease type 2M
Von Willebrand disease type 2N
Von Willebrand disease type 3