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Department

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

Afiliated experts

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