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Department

About the department

Department name (English): Department of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy

Department name (original): Pediatria, Fondazione IRCCS San Gerardo dei Tintori, Monza, ItaliaDay Hospital Talassemie ed emoglobinopatie

Subnetworks of expertise:

  • Hemochromatosis and other iron disorders
  • Red blood cell defects
  • Bone marrow failure

Healthcare provider: Fondazione IRCCS San Gerardo dei Tintori

Diseases covered by the department:

  • Acquired idiopathic sideroblastic anemia
  • Thrombocytopenia with congenital dyserythropoietic anemia
  • X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
  • Congenital amegakaryocytic thrombocytopenia
  • Rare anemia
  • Sideroblastic anemia
  • Constitutional sideroblastic anemia
  • Pearson syndrome
  • Mitochondrial myopathy and sideroblastic anemia
  • X-linked sideroblastic anemia and ataxia
  • Thiamine-responsive megaloblastic anemia syndrome
  • X-linked sideroblastic anemia
  • Autosomal recessive sideroblastic anemia
  • Severe congenital hypochromic anemia with ringed sideroblasts
  • Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay 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
  • Hereditary stomatocytosis
  • Overhydrated hereditary stomatocytosis
  • Dehydrated hereditary stomatocytosis
  • Constitutional hemolytic anemia due to acanthocytosis
  • Rare constitutional hemolytic anemia due to an enzyme disorder
  • 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
  • Class I glucose-6-phosphate dehydrogenase deficiency
  • Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder
  • 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
  • Rare acquired aplastic anemia
  • Idiopathic aplastic anemia
  • Red cell aplasia
  • Transient erythroblastopenia of childhood
  • Adult pure red cell aplasia
  • Rare deficiency anemia
  • Constitutional deficiency anemia
  • Constitutional anemia due to iron metabolism disorder
  • Congenital atransferrinemia
  • Aceruloplasminemia
  • Microcytic anemia with liver iron overload
  • IRIDA syndrome
  • Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder
  • Congenital intrinsic factor deficiency
  • Constitutional megaloblastic anemia due to folate metabolism disorder
  • Hereditary folate malabsorption
  • Constitutional megaloblastic anemia with severe neurologic disease
  • Vitamin B12- and folate-independent constitutional megaloblastic anemia
  • Rare acquired deficiency anemia
  • 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
  • L-ferritin deficiency
  • Rare hereditary hemochromatosis
  • HFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1) - OMIM 235200
  • HJV related hereditary hemochromatosis - OMIM 602390 (Hemochromatosis type 2A)
  • HAMP related hereditary hemochromatosis - OMIM 613313 (Hemochromatosis type 2B)
  • TFR2 related hereditary hemochromatosis OMIM 604250 (Hemochromatosis type 3)
  • FTH related hereditary hemochromatosis - OMIM 615517 (Hemochromatosis type 5)
  • Ferroportin Disease (Hemochromatosis type 4B)​
  • SLC40A1 related hereditary hemochromatosis - OMIM 606069 (Hemochromatosis type 4A)
  • Rare iron overload
  • Rare Ferritinopathy
  • Hereditary Hyperferritinemia with or without cataract
  • Hereditary hyperferritinemia with congenital cataracts
  • Genetic hyperferritinemia without iron overload
  • Neuroferritinopathy

Service offered

  • Diagnostics
  • Treatment and care

Patients covered

  • Pediatrics

Health professionals

Name Surname Academic title Charge