Name: Gian Luca
Academic title: Medical Doctor
Which is your area of expertise for the "Disease/group of diseases"?
Aceruloplasminemia Acquired idiopathic sideroblastic anemia Alpha- thalassaemia diseases Atypical hemolytic-uremic syndrome Beta-thalassemia and related diseases Congenital atransferrinemia Constitutional megaloblastic anemia Constitutional sideroblastic anemia (excluding Severe congenital hypochromic anemia with ringed sideroblasts) Hemoglobinopathy (Other than THAL and SCD) Hereditary elliptocytosis 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 Porphyrias Rare acquired deficiency anemia (Plummer-Vinson syndrome) 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 Sickle cell disease and related diseases
Which is your patient age coverage?
|English name||Original name||Subnetworks of expertise||Healthcare provider|
|Department of Medicine - Congenital Anemias and Iron Disemtabolism Center||Dipartimento di Medicina - Centro della Microcitemia, Anemie congenite e dismetabolismo del ferro||Hemochromatosis and other iron disorders, Red blood cell defects||E.O. Ospedali Galliera, Genova|