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Department

About the department

Department name (English): Pediatric Hematology and Oncology

Department name (original): Hematología y Oncología pediátrica

Subnetworks of expertise:

  • Myeloid malignancies
  • Lymphoid malignancies
  • Bleeding - Coagulation disorders
  • Red blood cell defects
  • Bone marrow failure

Healthcare provider: Hospital General Universitario Gregorio Marañón

Diseases covered by the department:

  • Tumor of hematopoietic and lymphoid tissues
  • Bloom syndrome
  • Deafness-lymphedema-leukemia syndrome
  • Mastocytosis
  • Systemic mastocytosis
  • Indolent systemic mastocytosis
  • Smouldering systemic mastocytosis
  • Isolated bone marrow mastocytosis
  • Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
  • Aggressive systemic mastocytosis
  • Lymphoadenopathic mastocytosis with eosinophilia
  • Mast cell leukemia
  • Classic mast cell leukemia
  • Aleukemic mast cell leukemia
  • Cutaneous mastocytosis
  • Cutaneous mastocytoma
  • Diffuse cutaneous mastocytosis
  • Bullous diffuse cutaneous mastocytosis
  • Pseudoxanthomatous diffuse cutaneous mastocytosis
  • Maculopapular cutaneous mastocytosis
  • Telangiectasia macularis eruptiva perstans
  • Typical urticaria pigmentosa
  • Plaque-form urticaria pigmentosa
  • Nodular urticaria pigmentosa
  • Mast cell sarcoma
  • Extracutaneous mastocytoma
  • Myeloid hemopathy
  • Acute myeloid leukemia
  • Acute myeloid leukemia with multilineage dysplasia
  • Therapy related acute myeloid leukemia and myelodysplastic syndrome
  • Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
  • Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor
  • Acute myeloid leukemia and myelodysplastic syndromes related to radiation
  • Acute leukemia of ambiguous lineage
  • Acute undifferentiated leukemia
  • Bilineal acute leukemia
  • Acute biphenotypic leukemia
  • Acute myeloid leukemia with recurrent genetic anomaly
  • Acute promyelocytic leukemia
  • Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
  • Acute myeloid leukemia with 11q23 abnormalities
  • Acute myeloid leukemia with t(8;21)(q22;q22) translocation
  • Acute myeloid leukemia with CEBPA somatic mutations
  • Acute myeloid leukemia with t(8;16)(p11;p13) translocation
  • Acute myeloid leukemia with t(6;9)(p23;q34)
  • Acute myeloid leukemia with t(9;11)(p22;q23)
  • Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)
  • Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
  • Acute myeloid leukemia with NPM1 somatic mutations
  • Unclassified acute myeloid leukemia
  • Acute erythroid leukemia
  • Acute megakaryoblastic leukemia
  • Acute megakaryoblastic leukemia in Down syndrome
  • Acute megakaryoblastic leukemia without Down syndrome
  • Acute panmyelosis with myelofibrosis
  • Acute basophilic leukemia
  • Myeloid sarcoma
  • Acute myeloid leukemia with minimal differentiation
  • Acute myeloblastic leukemia without maturation
  • Acute myeloblastic leukemia with maturation
  • Acute myelomonocytic leukemia
  • Acute monoblastic leukemia
  • Inherited acute myeloid leukemia
  • Inherited acute myeloid leukemia with presdisposing GAT2 mutation
  • Inherited acute myeloid leukemia with presdisposing RUNX1 mutation
  • Inherited acute myeloid leukemia with presdisposing DDX41 mutation
  • Myelodysplastic syndrome
  • Acquired idiopathic sideroblastic anemia
  • Refractory cytopenia with multilineage dysplasia
  • Refractory anemia
  • Unclassified myelodysplastic syndrome
  • Aregenerative anemia
  • Refractory anemia with excess blasts
  • Refractory anemia with excess blasts type 1
  • Refractory anemia with excess blasts type 2
  • Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
  • Refractory anemia with excess blasts in transformation
  • Myeloproliferative neoplasm
  • Essential thrombocythemia
  • Chronic myeloid leukemia
  • Primary myelofibrosis
  • Polycythemia vera
  • Chronic neutrophilic leukemia
  • Chronic myeloproliferative disease, unclassifiable
  • Chronic eosinophilic leukemia
  • Hypereosinophilic syndrome
  • Idiopathic hypereosinophilic syndrome
  • Primary hypereosinophilic syndrome
  • Secondary hypereosinophilic syndrome
  • Lymphocytic hypereosinophilic syndrome
  • Transient myeloproliferative syndrome
  • Hereditary thrombocytopenia with early-onset myelofibrosis
  • Myelodysplastic/myeloproliferative disease
  • Juvenile myelomonocytic leukemia
  • Chronic myelomonocytic leukemia
  • Atypical chronic myeloid leukemia
  • Unclassified myelodysplastic/myeloproliferative disease
  • Myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1
  • Myeloid neoplasm associated with PDGFRA rearrangement
  • Myeloid neoplasm associated with PDGFRB rearrangement
  • Myeloid neoplasm associated with FGFR1 rearrangement
  • Lymphoid hemopathy
  • Autoimmune lymphoproliferative syndrome
  • Plasma cell tumor
  • POEMS syndrome
  • Multiple myeloma
  • AL amyloidosis
  • Primary systemic amyloidosis
  • Primary localized amyloidosis
  • Plasmacytoma
  • Primary plasmacytoma of the bone
  • Extramedullary soft tissue plasmacytoma
  • Non-amyloid monoclonal immunoglobulin deposition disease
  • Heavy chain deposition disease
  • Light and heavy chain deposition disease
  • Light chain deposition disease
  • Heavy chain disease
  • Mu-heavy chain disease
  • Alpha-heavy chain disease
  • Gamma-heavy chain disease
  • Plasma cell leukemia
  • Immunodeficiency-associated lymphoproliferative disease
  • Post-transplant lymphoproliferative disease
  • Methotrexate-associated lymphoproliferative disorders
  • Lymphoproliferative disease associated with primary immune disease
  • Lymphoma
  • Non-Hodgkin lymphoma
  • Acute lymphoblastic leukemia
  • Precursor B-cell acute lymphoblastic leukemia
  • Precursor T-cell acute lymphoblastic leukemia
  • Mature B-cell acute lymphoblastic leukemia
  • B-cell non-Hodgkin lymphoma
  • Indolent B-cell non-Hodgkin lymphoma
  • Follicular lymphoma
  • Waldenström macroglobulinemia
  • Hairy cell leukemia
  • B-cell chronic lymphocytic leukemia
  • Indolent primary cutaneous B-cell lymphoma
  • Primary cutaneous marginal zone B-cell lymphoma
  • Primary cutaneous follicle center lymphoma
  • Hairy cell leukemia variant
  • Marginal zone lymphoma
  • MALT lymphoma
  • Splenic marginal zone lymphoma
  • Nodal marginal zone B-cell lymphoma
  • Splenic diffuse red pulp small B-cell lymphoma
  • Lymphoplasmacytic lymphoma without IgM production
  • Aggressive B-cell non-Hodgkin lymphoma
  • Burkitt lymphoma
  • Diffuse large B-cell lymphoma
  • Lymphomatoid granulomatosis
  • Primary mediastinal large B-cell lymphoma
  • Intravascular large B-cell lymphoma
  • Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly
  • Diffuse large B-cell lymphoma of the central nervous system
  • T-cell/histiocyte rich large B cell lymphoma
  • Diffuse large B-cell lymphoma with chronic inflammation
  • ALK-positive large B-cell lymphoma
  • Primary effusion lymphoma
  • Mantle cell lymphoma
  • B-cell prolymphocytic leukemia
  • Aggressive primary cutaneous B-cell lymphoma
  • Primary cutaneous diffuse large B-cell lymphoma, leg type
  • Plasmablastic lymphoma
  • T-cell non-Hodgkin lymphoma
  • CD4+/CD56+ hematodermic neoplasm
  • T-cell prolymphocytic leukemia
  • T-cell large granular lymphocyte leukemia
  • Aggressive NK-cell leukemia
  • Adult T-cell leukemia/lymphoma
  • Extranodal nasal NK/T cell lymphoma
  • Enteropathy-associated T-cell lymphoma
  • Hepatosplenic T-cell lymphoma
  • Angioimmunoblastic T-cell lymphoma
  • Anaplastic large cell lymphoma
  • ALK-positive anaplastic large cell lymphoma
  • ALK-negative anaplastic large cell lymphoma
  • Primary cutaneous T-cell lymphoma
  • Indolent primary cutaneous T-cell lymphoma
  • Primary cutaneous CD30+ T-cell lymphoproliferative disease
  • Lymphomatoid papulosis
  • Primary cutaneous anaplastic large cell lymphoma
  • Subcutaneous panniculitis-like T-cell lymphoma
  • Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma
  • Mycosis fungoides and variants
  • Classic mycosis fungoides
  • Granulomatous slack skin
  • Folliculotropic mycosis fungoides
  • Localized pagetoid reticulosis
  • Aggressive primary cutaneous T-cell lymphoma
  • Sézary syndrome
  • Primary cutaneous peripheral T-cell lymphoma not otherwise specified
  • Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma
  • Primary cutaneous gamma/delta-positive T-cell lymphoma
  • Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood
  • Hydroa vacciniforme-like lymphoma
  • Peripheral T-cell lymphoma NOS
  • Hodgkin lymphoma
  • Classic Hodgkin lymphoma
  • Classic Hodgkin lymphoma, nodular sclerosis type
  • Classic Hodgkin lymphoma, mixed cellularity type
  • Classic Hodgkin lymphoma, lymphocyte-rich type
  • Classic Hodgkin lymphoma, lymphocyte-depleted type
  • Nodular lymphocyte predominant Hodgkin lymphoma
  • Composite lymphoma
  • Primary organ-specific lymphoma
  • Primary pulmonary lymphoma
  • Primary cutaneous lymphoma
  • Primary cutaneous B-cell lymphoma
  • Primary central nervous system lymphoma
  • Thyroid lymphoma
  • Primary oculocerebral lymphoma
  • Primary intraocular lymphoma
  • Primary bone lymphoma
  • Primary lymphoma of the conjunctiva
  • RAS-associated autoimmune leukoproliferative disease
  • Persistent polyclonal B-cell lymphocytosis
  • Castleman disease
  • Pediatric Castleman disease
  • Localized Castleman disease
  • Multicentric Castleman disease
  • Polycythemia
  • Primary familial polycythemia
  • Secondary polycythemia
  • Congenital secondary polycythemia
  • Chuvash erythrocytosis
  • Autosomal recessive secondary polycythemia not associated with VHL gene
  • Autosomal dominant secondary polycythemia
  • Acquired secondary polycythemia
  • Gaisböck syndrome
  • Rare coagulation disorder
  • Rare thrombotic disease of hematologic origin
  • Rare thrombotic disorder due to a coagulation factors defect
  • Rare thrombotic disorder due to a constitutional coagulation factors defect
  • Congenital factor XII deficiency
  • Familial thrombomodulin anomalies
  • Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
  • Rare hereditary thrombophilia
  • Hereditary thrombophilia due to congenital protein S deficiency
  • Hereditary thrombophilia due to congenital protein C deficiency
  • Hereditary thrombophilia due to congenital antithrombin deficiency
  • Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
  • Rare thrombotic disorder due to an acquired coagulation factors defect
  • Catastrophic antiphospholipid syndrome
  • Heparin-induced thrombocytopenia
  • Protein S acquired deficiency
  • Acquired purpura fulminans
  • Simple cryoglobulinemia
  • Rare thrombotic disorder due to a platelet anomaly
  • Thrombotic thrombocytopenic purpura
  • Congenital thrombotic thrombocytopenic purpura
  • Acquired thrombotic thrombocytopenic purpura
  • Rare thrombotic disorder due to a constitutional platelet anomaly
  • Familial thrombocytosis
  • Hereditary thrombocytosis with transverse limb defect
  • Rare thrombotic disorder due to an acquired platelet anomaly
  • Rare hemorrhagic disorder
  • Rare hemorrhagic disorder due to a coagulation factors defect
  • Rare hemorrhagic disorder due to a constitutional coagulation factors defect
  • Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
  • Hemophilia
  • Hemophilia A
  • Severe hemophilia A
  • Moderately severe hemophilia A
  • Mild hemophilia A
  • Symptomatic form of hemophilia A in female carriers
  • Hemophilia B
  • Severe hemophilia B
  • Moderately severe hemophilia B
  • Mild hemophilia B
  • Symptomatic form of hemophilia B in female carriers
  • Congenital factor V deficiency
  • Congenital fibrinogen deficiency
  • Familial afibrinogenemia
  • Familial dysfibrinogenemia
  • Familial hypofibrinogenemia
  • Familial hypodysfibrinogenemia
  • Congenital alpha2-antiplasmin deficiency
  • Congenital factor XIII deficiency
  • Von Willebrand disease
  • Von Willebrand disease type 1
  • Von Willebrand disease type 2
  • Von Willebrand disease type 2A
  • Von Willebrand disease type 2B
  • Von Willebrand disease type 2M
  • Von Willebrand disease type 2N
  • Von Willebrand disease type 3
  • Congenital factor XI deficiency
  • Congenital plasminogen activator inhibitor type 1 deficiency
  • Congenital high-molecular-weight kininogen deficiency
  • Congenital prekallikrein deficiency
  • Combined deficiency of factor V and factor VIII
  • Congenital vitamin K-dependent coagulation factors deficiency
  • Congenital factor VII deficiency
  • Congenital factor II deficiency
  • Congenital factor X deficiency
  • Hereditary combined deficiency of vitamin K-dependent clotting factors
  • Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
  • East Texas bleeding disorder
  • Thrombomodulin-related bleeding disorder
  • Rare hemorrhagic disorder due to an acquired coagulation factor defect
  • Acquired prothrombin deficiency
  • Acquired hemophilia
  • Acquired von Willebrand syndrome
  • Rare hemorrhagic disorder due to a platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional thrombocytopenia
  • Syndromic constitutional thrombocytopenia
  • Stormorken-Sjaastad-Langslet syndrome
  • Thrombocytopenia-absent radius syndrome
  • Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
  • MYH9-related disease
  • GNE myopathy
  • Jacobsen syndrome
  • Macrothrombocytopenia with mitral valve insufficiency
  • Alpha delta granule deficiency
  • Dense granule disease
  • Wiskott-Aldrich syndrome
  • Chédiak-Higashi syndrome
  • Hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome
  • Hermansky-Pudlak syndrome
  • Hermansky-Pudlak syndrome with neutropenia
  • Hermansky-Pudlak syndrome with pulmonary fibrosis
  • Hermansky-Pudlak syndrome without pulmonary fibrosis
  • Hermansky-Pudlak syndrome type 7
  • Hermansky-Pudlak syndrome type 8
  • Hermansky-Pudlak syndrome type 9
  • Isolated constitutional thrombocytopenia
  • Isolated hereditary giant platelet disorder
  • Severe autosomal recessive macrothrombocytopenia
  • Bernard-Soulier syndrome
  • Thrombocytopenia with congenital dyserythropoietic anemia
  • Autosomal dominant macrothrombocytopenia
  • Alpha granule disease
  • Gray platelet syndrome
  • Quebec platelet disorder
  • Medich giant platelet syndrome
  • White platelet syndrome
  • Paris-Trousseau thrombocytopenia
  • X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
  • Hereditary thrombocytopenia with normal platelets
  • X-linked thrombocytopenia with normal platelets
  • Autosomal thrombocytopenia with normal platelets
  • Congenital amegakaryocytic thrombocytopenia
  • Bleeding diathesis due to thromboxane synthesis deficiency
  • Isolated delta-storage pool disease
  • Autosomal dominant thrombocytopenia with platelet secretion defect
  • Rare hemorrhagic disorder due to a qualitative platelet defect
  • Glanzmann thrombasthenia
  • Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
  • Ehlers-Danlos syndrome, fibronectinemic type
  • Scott syndrome
  • P2Y12 defect
  • Pseudo-von Willebrand disease
  • Bleeding diathesis due to a collagen receptor defect
  • Bleeding diathesis due to glycoprotein VI deficiency
  • Bleeding diathesis due to integrin alpha2-beta1 deficiency
  • Bleeding disorder due to CalDAG-GEFI deficiency
  • Rare hemorrhagic disorder due to an acquired platelet anomaly
  • Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
  • TAFRO syndrome
  • HELLP syndrome
  • Fetal and neonatal alloimmune thrombocytopenia
  • Autoimmune thrombocytopenia
  • Immune thrombocytopenic purpura
  • Evans syndrome
  • STAT3-related early-onset multisystem autoimmune disease
  • Kasabach-Merritt syndrome
  • 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
  • Atypical hemolytic-uremic syndrome
  • Atypical hemolytic-uremic syndrome with DGKE deficiency
  • Atypical hemolytic-uremic syndrome with C3 anomaly
  • Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly
  • Atypical hemolytic-uremic syndrome with B factor anomaly
  • Atypical hemolytic-uremic syndrome with H factor anomaly
  • Atypical hemolytic-uremic syndrome with I factor anomaly
  • Atypical hemolytic-uremic syndrome with anti-factor H antibodies
  • Atypical hemolytic-uremic syndrome with thrombomodulin anomaly
  • 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
  • Typical hemolytic-uremic syndrome
  • 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 e-mail: elena.cela(ELIMINAR)@salud.madrid.org

Department phone number: +34915290037/2

Related departments

Hematology

Health professionals

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