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Corti, Paola

About me

Name: Paola

Surname: Corti

Academic title: Md, Phd


Which is your area of expertise for the "Disease/group of diseases"?

  • Treatment and care

Disease groups:

Aceruloplasminemia Acquired idiopathic sideroblastic anemia Acquired red cell aplasia Alpha- thalassaemia diseases Beta-thalassemia and related diseases Blackfan-Diamond anemia Congenital atransferrinemia Congenital dyserythropoietic anemia Constitutional megaloblastic anemia Constitutional sideroblastic anemia (excluding Severe congenital hypochromic anemia with ringed sideroblasts) Dyskeratosis congenita and related disorders Fanconi anemia Hemoglobinopathy (Other than THAL and SCD) Hereditary elliptocytosis Hereditary Hyperferritinemia with or without cataract (OMIM 600886) Hereditary spherocytosis Hereditary stomatocytosis HFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1 - OMIM 235201) Iron-refractory iron deficiency anemia syndrome Microcytic anemia with liver iron overload Myelodysplastic syndrome Myeloproliferative neoplasm (Other than Chronic myeloid leukemia and Primary myelofibrosis) Paroxysmal nocturnal hemoglobinuria Rare acquired aplastic anemia (Other than PNH) Rare acquired deficiency anemia (Plummer-Vinson syndrome) Rare constitutional aplastic anemia (Other than BDA, DKC, FA, SDS) Rare constitutional hemolytic anemia due to an enzyme disorder (Other than PKD) Rare constitutional hemolytic anemia due to pyruvate kinase deficiency Rare hereditary hemochromatosis (Other than Type 1) Severe congenital hypochromic anemia with ringed sideroblasts Shwachman-Diamond syndrome Sickle cell disease and related diseases

Which is your patient age coverage?

  • Pediatrics


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