About the department
Department name (English): Department of Pediatric Hematology and Oncology
Department name (original): Pädiatrische Hämatologie und Onkologie
Subnetworks of expertise:
Healthcare provider: Gemeinschaftsklinikum Mittelrhein gGmbH
Diseases covered by the department:
- 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
- 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
- Familial pseudohyperkalemia
- Southeast Asian ovalocytosis
- Hereditary cryohydrocytosis with reduced stomatin
- Hereditary cryohydrocytosis with normal stomatin
- Constitutional hemolytic anemia due to acanthocytosis
- Abetalipoproteinemia
- McLeod neuroacanthocytosis syndrome
- Primary CD59 deficiency
- Rare constitutional hemolytic anemia due to an enzyme disorder
- Congenital erythropoietic porphyria
- Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies
- Glutathione synthetase deficiency
- Glutathione synthetase deficiency with 5-oxoprolinuria
- Glutathione synthetase deficiency without 5-oxoprolinuria
- Gamma-glutamylcysteine synthetase deficiency
- Hemolytic anemia due to glutathione reductase deficiency
- 6-phosphogluconate dehydrogenase deficiency
- Hemolytic anemia due to a disorder of glycolytic enzymes
- Glycogen storage disease due to muscle phosphofructokinase deficiency
- Triose phosphate-isomerase deficiency
- Glycogen storage disease due to aldolase A deficiency
- Glycogen storage disease due to phosphoglycerate kinase 1 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