Departments

About the department

Department name (English): Department of Pediatrics

Department name (original): Kinderklinik und Poliklinik

Subnetworks of expertise:

• Bleeding - Coagulation disorders
• Red blood cell defects

Healthcare provider: Universitätsklinikum Würzburg

Diseases covered by the department:

• Essential thrombocythemia
• Rare coagulation disorder
• Rare thrombotic disease of hematologic origin
• Rare thrombotic disorder due to a coagulation factors defect
• Rare thrombotic disorder due to a constitutional coagulation factors defect
• Congenital factor XII deficiency
• Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• Rare hereditary thrombophilia
• Hereditary thrombophilia due to congenital protein S deficiency
• Hereditary thrombophilia due to congenital protein C deficiency
• Rare thrombotic disorder due to an acquired coagulation factors defect
• Catastrophic antiphospholipid syndrome
• Heparin-induced thrombocytopenia
• Protein S acquired deficiency
• Rare thrombotic disorder due to a platelet anomaly
• Thrombotic thrombocytopenic purpura
• Congenital thrombotic thrombocytopenic purpura
• Acquired thrombotic thrombocytopenic purpura
• Rare thrombotic disorder due to a constitutional platelet anomaly
• Familial thrombocytosis
• Hereditary thrombocytosis with transverse limb defect
• Rare thrombotic disorder due to an acquired platelet anomaly
• Rare hemorrhagic disorder
• Rare hemorrhagic disorder due to a coagulation factors defect
• Rare hemorrhagic disorder due to a constitutional coagulation factors defect
• Hemophilia
• Hemophilia A
• Hemophilia B
• Congenital factor V deficiency
• Congenital fibrinogen deficiency
• Familial afibrinogenemia
• Familial dysfibrinogenemia
• Familial hypofibrinogenemia
• Familial hypodysfibrinogenemia
• Congenital factor XIII deficiency
• Von Willebrand disease
• Von Willebrand disease type 1
• Von Willebrand disease type 2
• Von Willebrand disease type 3
• Congenital factor XI deficiency
• Combined deficiency of factor V and factor VIII
• Congenital vitamin K-dependent coagulation factors deficiency
• Hereditary combined deficiency of vitamin K-dependent clotting factors
• Rare hemorrhagic disorder due to an acquired coagulation factor defect
• Acquired von Willebrand syndrome
• Rare hemorrhagic disorder due to a platelet anomaly
• Rare hemorrhagic disorder due to a constitutional platelet anomaly
• Rare hemorrhagic disorder due to a constitutional thrombocytopenia
• Syndromic constitutional thrombocytopenia
• Isolated constitutional thrombocytopenia
• Rare hemorrhagic disorder due to a qualitative platelet defect
• Glanzmann thrombasthenia
• Scott syndrome
• P2Y12 defect
• Pseudo-von Willebrand disease
• Bleeding diathesis due to a collagen receptor defect
• Bleeding disorder due to CalDAG-GEFI deficiency
• Rare hemorrhagic disorder due to an acquired platelet anomaly
• Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
• HELLP syndrome
• Fetal and neonatal alloimmune thrombocytopenia
• Autoimmune thrombocytopenia
• Immune thrombocytopenic purpura
• Evans syndrome
• Kasabach-Merritt syndrome
• Rare anemia
• Hemoglobinopathy
• Hemoglobin E disease
• Hemoglobin D disease
• Unstable hemoglobin disease
• Alpha-thalassemia and related diseases
• Alpha-thalassemia
• Hemoglobin H disease
• Hb Bart's hydrops fetalis
• Alpha-thalassemia-related diseases
• Alpha-thalassemia-X-linked intellectual disability syndrome
• Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
• Alpha-thalassemia-myelodysplastic syndrome
• Beta-thalassemia and related diseases
• Beta-thalassemia
• Beta-thalassemia major
• Beta-thalassemia intermedia
• Dominant beta-thalassemia
• Beta-thalassemia associated with another hemoglobin anomaly
• Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
• Delta-beta-thalassemia
• Hemoglobin C-beta-thalassemia syndrome
• Hemoglobin E-beta-thalassemia syndrome
• Hemoglobin Lepore-beta-thalassemia syndrome
• Beta-thalassemia with other manifestations
• Beta-thalassemia-X-linked thrombocytopenia syndrome
• Sickle cell disease and related diseases
• Sickle cell anemia
• Sickle cell disease associated with an other hemoglobin anomaly
• Sickle cell-beta-thalassemia disease syndrome
• Sickle cell-hemoglobin C disease syndrome
• Sickle cell-hemoglobin D disease syndrome
• Sickle cell-hemoglobin E disease syndrome
• Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
• Hemoglobinopathy Toms River
• Hereditary methemoglobinemia
• Hemoglobin C disease
• Hemoglobin M disease
• Acquired methemoglobinemia
• Rare hemolytic anemia
• Rare constitutional hemolytic anemia
• Atypical hemolytic-uremic syndrome
• Rare constitutional hemolytic anemia due to a red cell membrane anomaly
• Hereditary spherocytosis
• Hereditary elliptocytosis
• Distal renal tubular acidosis with anemia
• Hereditary stomatocytosis
• Overhydrated hereditary stomatocytosis
• Dehydrated hereditary stomatocytosis
• Rh deficiency syndrome
• Southeast Asian ovalocytosis
• Constitutional hemolytic anemia due to acanthocytosis
• McLeod neuroacanthocytosis syndrome
• Rare constitutional hemolytic anemia due to an enzyme disorder
• Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies
• Hemolytic anemia due to glutathione reductase deficiency
• 6-phosphogluconate dehydrogenase deficiency
• Hemolytic anemia due to a disorder of glycolytic enzymes
• Triose phosphate-isomerase deficiency
• Hemolytic anemia due to red cell pyruvate kinase deficiency
• Hemolytic anemia due to glucophosphate isomerase deficiency
• Hemolytic anemia due to diphosphoglycerate mutase deficiency
• Non-spherocytic hemolytic anemia due to hexokinase deficiency
• Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
• Class I glucose-6-phosphate dehydrogenase deficiency
• Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder
• Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
• Hemolytic anemia due to adenylate kinase deficiency
• Hemolytic anemia due to erythrocyte adenosine deaminase overproduction
• Heinz body anemia
• Rare acquired hemolytic anemia
• Typical hemolytic-uremic syndrome

Service offered

• Prevention and genetic counseling
• Diagnostics
• Treatment and care

Patients covered

• Pediatrics