Departments

About the department

Department name (English):  Pediatric Oncology and Hematology Department

Department name (original): Servicio de Oncología y Hematología Pediátricas

Subnetworks of expertise:

• Red blood cell defects
• Bone marrow failure

Healthcare provider: Hospital Universitari Vall d'Hebron

Diseases covered by the department:

• Hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome
• Thrombocytopenia with congenital dyserythropoietic anemia
• X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
• Autosomal thrombocytopenia with normal platelets
• Congenital amegakaryocytic thrombocytopenia
• Rare anemia
• Thiamine-responsive megaloblastic anemia syndrome
• 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
• Rare acquired hemolytic anemia
• Paroxysmal nocturnal hemoglobinuria
• Aplastic anemia
• Rare constitutional aplastic anemia
• Blackfan-Diamond anemia
• Dyskeratosis congenita
• Fanconi anemia
• Revesz syndrome
• Hoyeraal-Hreidarsson syndrome
• WT limb-blood syndrome
• Shwachman-Diamond syndrome
• Autosomal dominant aplasia and myelodysplasia
• Hereditary isolated aplastic anemia
• Pancytopenia-developmental delay syndrome
• Rare acquired aplastic anemia
• Idiopathic aplastic anemia
• Red cell aplasia
• Transient erythroblastopenia of childhood
• Adult pure red cell aplasia
• Monocytopenia with susceptibility to infections
• Rare deficiency anemia
• Constitutional deficiency anemia
• Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder
• Methylmalonic acidemia with homocystinuria
• Methylmalonic acidemia with homocystinuria, type cblC
• Methylmalonic acidemia with homocystinuria, type cblD
• Methylmalonic acidemia with homocystinuria type cblF
• Methylmalonic acidemia with homocystinuria, type cblJ
• Methylmalonic acidemia with homocystinuria, type cblX
• Transcobalamin deficiency
• Congenital intrinsic factor deficiency
• Homocystinuria without methylmalonic aciduria
• Methylcobalamin deficiency type cblE
• Methylcobalamin deficiency type cblG
• Methylcobalamin deficiency type cblDv1
• Gräsbeck-Imerslund disease
• Constitutional megaloblastic anemia due to folate metabolism disorder
• Formiminoglutamic aciduria
• Hereditary folate malabsorption
• Constitutional megaloblastic anemia with severe neurologic disease
• Vitamin B12- and folate-independent constitutional megaloblastic anemia
• Hereditary orotic aciduria
• Hypoxanthine-guanine phosphoribosyltransferase deficiency
• Lesch-Nyhan syndrome
• Hypoxanthine guanine phosphoribosyltransferase partial deficiency
• Constitutional dyserythropoietic anemia
• Congenital dyserythropoietic anemia
• Congenital dyserythropoietic anemia type I
• Congenital dyserythropoietic anemia type III
• Congenital dyserythropoietic anemia type II
• Congenital dyserythropoietic anemia type IV
• Majeed syndrome
• Pancreatic insufficiency-anemia-hyperostosis syndrome

Service offered

• Prevention and genetic counseling
• Diagnostics
• Treatment and care

Patients covered

• Pediatrics

Department phone number: +34934893093