Klinik für Kinder- und Jugendmedizin am Eltern-Kind-Zentrum Prof. Hess des Klinikums Bremen-Mitte Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome
Autoimmune interstitial lung disease-arthritis syndrome
Autosomal dominant polycystic kidney disease
Autosomal recessive polycystic kidney disease
Bardet-Biedl syndrome
Bartter syndrome
Biotinidase deficiency
Bleeding disorder in hemophilia A carriers
Bleeding disorder in hemophilia B carriers
C3 glomerulonephritis
CREST syndrome
Carbamoyl-phosphate synthetase 1 deficiency
Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy
Citrullinemia
Cystic fibrosis
Cystinosis
Dent disease
Denys-Drash syndrome
Diffuse cutaneous systemic sclerosis
Enthesitis-related juvenile idiopathic arthritis
Eosinophilic fasciitis
Fabry disease
Galactosemia
Gaucher disease
Genetic steroid-resistant nephrotic syndrome
Glycogen storage disease
Hemophilia
Hemophilia A
Hemophilia B
Idiopathic steroid-resistant nephrotic syndrome
Idiopathic steroid-sensitive nephrotic syndrome
Immunoglobulin A vasculitis
Jeune syndrome
Juvenile dermatomyositis
Juvenile idiopathic arthritis
Juvenile polymyositis
Limited systemic sclerosis
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium chain acyl-CoA dehydrogenase deficiency
Mild hemophilia A
Mild hemophilia B
Mixed connective tissue disease
Moderate hemophilia A
Moderate hemophilia B
Motor neuron disease
Mucolipidosis
Mucopolysaccharidosis
Multicystic dysplastic kidney
Muscular channelopathy
Neonatal dermatomyositis
Neonatal lupus erythematosus
Neonatal scleroderma
Neuromuscular disease
Neuromuscular junction disease
Oligoarticular juvenile idiopathic arthritis
Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies
Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies
Ornithine transcarbamylase deficiency
Osteochondrosis
Overlapping connective tissue disease
PLCG2-associated antibody deficiency and immune dysregulation
Pediatric Castleman disease
Pediatric systemic lupus erythematosus
Phenylketonuria
Polyarticular juvenile idiopathic arthritis
Primary membranoproliferative glomerulonephritis
Propionic acidemia
Psoriasis-related juvenile idiopathic arthritis
Rare hypercholesterolemia
Rare pediatric systemic disease
Renal dysplasia
Renal hypoplasia
Renal or urinary tract malformation
Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis
Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis
STAT3-related early-onset multisystem autoimmune disease
Sarcoidosis
Secondary neonatal autoimmune disease
Severe hemophilia A
Severe hemophilia B
Short chain acyl-CoA dehydrogenase deficiency
Skeletal muscle disease
Systemic lupus erythematosus
Systemic sclerosis
Systemic-onset juvenile idiopathic arthritis
Tubulointerstitial nephritis and uveitis syndrome
Unexplained long-lasting fever/inflammatory syndrome
Unspecified juvenile idiopathic arthritis
Very long chain acyl-CoA dehydrogenase deficiency
Waardenburg syndrome