Departments

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