Departments

Information

About the department

Department name (English): Brussels Academic Hospital Laboratory

Department name (original): Laboratoire Hospitalier Universitaire de Bruxelles – Universitair Laboratorium Brussel

Subnetworks of expertise:

Myeloid malignancies
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
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
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
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