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About the department

Department name (English): University Laboratory department

Department name (original): LHUB-ULB

Subnetworks of expertise:

  • Red blood cell defects

Healthcare provider: CUB-Hôpital Erasme

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
  • Familial pseudohyperkalemia
  • Southeast Asian ovalocytosis
  • Hereditary cryohydrocytosis with reduced stomatin
  • Hereditary cryohydrocytosis with normal stomatin
  • Constitutional hemolytic anemia due to acanthocytosis
  • 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
  • 6-phosphogluconate dehydrogenase deficiency
  • Hemolytic anemia due to a disorder of glycolytic enzymes
  • Hemolytic anemia due to red cell pyruvate kinase deficiency
  • Hemolytic anemia due to glucophosphate isomerase deficiency
  • Non-spherocytic hemolytic anemia due to hexokinase 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 erythrocyte adenosine deaminase overproduction
  • Heinz body anemia

Service offered

  • Prevention and genetic counseling
  • Diagnostics

Patients covered

  • Pediatrics
  • Adults
  • Ageing

Department e-mail: secretariatan(ELIMINAR)

Department phone number: +324352000

Laboratory - Clinical Chemistry and Haematology

Health professionals

Name Surname Academic title Charge